Methods and products for treating inflammation

ABSTRACT

Pharmaceutical compositions comprising an isolated form of a compound of Formula I or IA (e.g., anatabine or S-(−)-anatabine) or a salt thereof can be used to treat disorders comprising an inflammatory component, including chronic, low-level inflammation. Compounds of Formula I also can be provided, for example, in other vehicles such as beverage products and consumer products such as lotions and creams.

This application claims the benefit of and incorporates by referenceSer. No. 61/383,811 filed Sep. 17, 2010; Ser. No. 61/384,447 filed Sep.20, 2010; Ser. No. 61/439,473 filed Feb. 4, 2011; Ser. No. 61/480,271filed Apr. 28, 2011; and Ser. No. 61/480,258 filed Apr. 28, 2011.

Each reference cited in this disclosure is incorporated herein in itsentirety.

TECHNICAL FIELD

This disclosure relates generally to methods and compositions fortreating inflammation and conditions associated with inflammation.

BACKGROUND

Inflammation is a protective response to harmful stimuli, such asoxidative stress, irritants, pathogens, and damaged cells. Theinflammatory response involves the production and release ofinflammatory modulators that heal injured tissue and destroy damagedcells, by directly or indirectly producing and/or signaling the releaseof agents that produce reactive oxygen species. Thus, an appropriateinflammatory response involves a balance between the destruction ofdamaged cells and the healing of injured tissue.

An unchecked inflammatory response can lead to oxidative stress and theonset of various inflammatory disease pathologies. In fact, inflammatoryprocesses underlie a wide variety of pathologies, including immune andautoimmune diseases, gastrointestinal diseases, various types of cancer,vascular disorders, heart disease, and neurodegenerative diseases. Thereis a need in the art for agents that can reduce inappropriate levels ofinflammation.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. Graph showing effects of anatabine on TNFα-induced NFκB activityin vitro. See Example 1.

FIG. 2. Graph showing effects of a crude extract of smokeless tobacco onTNFα-induced NFκB activity in vitro. See Example 1.

FIG. 3. Graph showing effects of nicotine and of an alkaloid extract ofsmokeless tobacco on TNFα-induced NFκB activity in vitro. See Example 1.

FIG. 4. Graph showing the results of a cytotoxicity assay measuringrelease of lactate dehydrogenase (LDH) using supernatant from the cellsassayed in FIG. 1. See Example 2.

FIG. 5. Graph showing the results of a cytotoxicity assay usingsupernatant from the cells assayed in FIG. 2. See Example 2.

FIG. 6. Graph showing the results of a cytotoxicity assay usingsupernatant from the cells assayed in FIG. 3. See Example 2.

FIG. 7. Graph showing concentrations in rat plasma as a function of timeof anatabine and nicotine after a single intravenous bolus injection.

FIG. 8. Graph showing concentrations of anatabine and nicotine in ratplasma as a function of time (semi-log).

FIG. 9. Graph showing AUC_(0→∞) versus dose for both anatabine andnicotine in male and female rats.

FIG. 10. Graph showing concentrations of anatabine or nicotine in ratbrain extracts following a single intravenous bolus dose.

FIG. 11. Graph showing mean concentration of anatabine and nicotine inrat brain extracts 0.5 hours after a single intravenous bolus dose.

FIG. 12. Nicotine product ion scan.

FIG. 13. Nicotine sample chromatogram.

FIG. 14. Anatabine product ion scan.

FIG. 15. Anatabine sample chromatogram.

FIG. 16. Nicotine-d3 product ion scan.

FIG. 17. Nicotine-d3 sample chromatogram.

FIG. 18. Anatabine-d4 product ion scan.

FIG. 19. Anatabine-d4 sample chromatogram.

FIG. 20. Graph showing mean body weights (±Std Dev) for each treatmentgroup and gender.

FIGS. 21A-21B. Graphs showing mean (±SEM) concentration of anatabine inplasma for male or female rats. FIG. 21A, 0.6 mg/kg body weight (BW);FIG. 21B, 6.0 mg/kg BW.

FIGS. 22A-22B. Graphs showing mean (±SEM) concentration of anatabine inplasma for male and female rats combined. FIG. 22A, 0.6 mg/kg BW; FIG.22B, 6.0 mg/kg BW.

FIGS. 23A-23B. Graphs showing mean (±SEM), maximal (Cp, max), andminimal (Cp, min) concentrations of anatabine in plasma for male orfemale rats. FIG. 23A, 0.6 mg/kg BW; FIG. 23B, 6.0 mg/kg BW.

FIGS. 24A-C. Graphs showing concentration-response relationships of thepositive controls on activation (Ach), potentiation (epibatidine), orinhibition (MLA) of the nAChR α3/β4 channel. FIG. 24A, Ach; FIG. 24B,epibatidine; FIG. 24C, MLA.

FIGS. 25A-B. Graphs showing concentration-response relationships of thetest articles on activation of the nAChR α3/β4 channel. FIG. 25A,nicotine (−) isomer; FIG. 25B, anatabine.

FIGS. 26A-B. Graphs showing concentration-response relationships of thetest articles on inhibition of the nAChR α3/β4 channel. FIG. 26A,anatabine; FIG. 26B, nicotine.

FIGS. 27A-C. Graphs showing concentration-response relationships ofpositive controls on activation (Ach), potentiation (epibatidine), orinhibition (MLA) of the nAChR α4/β2 channel. FIG. 27A, Ach; FIG. 27B,epibatidine and Ach; FIG. 27C, MLA, Ach, and epibatidine.

FIGS. 28A-B. Graphs showing concentration-response relationships of testarticles on activation of the nAChR α4/β2 channel. FIG. 28A, anatabine;FIG. 28B, nicotine (−) isomer.

FIGS. 29A-B. Graphs showing concentration-response relationships of testarticles on inhibition of the nAChR α4/β2 channel. FIG. 29A, anatabine;FIG. 29B, nicotine (−) isomer.

FIGS. 30A-B. Graphs showing concentration-response relationships ofpositive controls on activation (Ach) and inhibition (MLA) of the nAChRα7 channel. FIG. 30A, PNU and Ach; FIG. 30B, MLA and Ach.

FIGS. 31A-B. Graphs showing concentration-response relationships of testarticles on activation of the nAChR α7 channel. FIG. 31A, anatabine;FIG. 31B, nicotine (−) isomer.

FIGS. 32A-B. Graphs showing concentration-response relationships of testarticles on inhibition of the nAChR α7 channel: FIG. 32A, anatabine;FIG. 32B, nicotine (−) isomer.

FIG. 33. Graph showing effect of anatabine (“RCP006”) (30 minutes) onBACE-1 mRNA expression in human neuronal SHSY cells.

FIG. 34. Western blots and graph showing effect of anatabine (“RCP006”)(24 hours) on BACE-1 protein expression in human neuronal SHSY cells.

FIGS. 35A-B. Graphs showing the effect of anatabine (“RCP006”) on Aβproduction in 7W CHO cells. FIG. 35A, Aβ1-42. FIG. 35B, Aβ1-40.

FIG. 36. Graph showing the effect of anatabine (“RCP006”) on sAPPβ/sAPPαproduction in 7W CHO cells.

FIG. 37. Graph demonstrating lack of observed toxicity of anatabine(“RCP006”) in 7W CHO cells.

FIG. 38. Graph demonstrating that anatabine (“RCP006”) inhibits NFκBactivation in the brain of wild-type mice.

FIG. 39. Graph demonstrating the effect of anatabine (“RCP006”) on theinhibition of IL-1β release after LPS stimulation in whole human blood.

FIG. 40. Graph comparing the anti-inflammatory effects (IL-1βinhibition) of anatabine (“RCP006”) and NSAIDs after treatment of wholehuman blood with LPS.

FIG. 41. Graph demonstrating the anti-inflammatory effect of anatabine(“RCP006”) on LPS-induced IL-1β release in human blood over time.

FIG. 42. Graph demonstrating thyroid pathology score, expressed aspercent of the thyroid area infiltrated by lymphocytes and damaged, incontrol mice and anatabine-treated mice. p=0.05.

FIGS. 43A-B. Photomicrographs of thyroids of control mouse (FIG. 43A)and mouse treated with anatabine (FIG. 43B).

FIG. 44. Graph demonstrating levels of antibodies to PPD (purifiedprotein derivative) in control and anatabine-treated mice.

FIG. 45. Graph demonstrating levels of antibodies to thyroglobulin onday 7 in control and anatabine-treated mice.

FIG. 46. Graph demonstrating levels of antibodies to thyroglobulin onday 14 in control and anatabine-treated mice.

FIG. 47. Graph demonstrating levels of antibodies to thyroglobulin onday 21 in control and anatabine-treated mice.

FIG. 48. Graph demonstrating that anatabine-treated mice have feweractivated T cells than control mice.

FIG. 49. Graph demonstrating that anatabine-treated mice have fewer Tregulatory cells than control mice.

FIG. 50. Graph demonstrating that anatabine-treated mice appear to havelower antigen-presentation ability than control mice.

FIG. 51. Graph demonstrating thyroid histopathology in control andanatabine-treated mice.

FIG. 52. Graph showing effect of S-(−)-anatabine on TNFα-induced NFκBactivity in vitro.

DETAILED DESCRIPTION

This disclosure describes methods of using a composition comprising anisolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof to treat disorders comprising aninflammatory component, including chronic, low-level inflammation.“Treat” as used herein refers to reducing a symptom of the inflammationor resulting disorder but does not require complete cure, either of theinflammation or the disorder. “Reduction of a symptom” of a disorderwith an NFκB-mediated inflammatory component includes but is not limitedto elimination of the symptom, reduction in frequency, severity, orduration of the symptom, and delaying onset of the symptom. Accordingly,compositions comprising an isolated form of a compound of Formula I orIA (e.g., anatabine or S-(−)-anatabine) or a salt thereof can beadministered to individuals before or after manifestation of a symptom.Symptoms include, but are not limited to, subjective indications (e.g.,pain or swelling) as well as objective indications detectable withlaboratory tests (e.g., an elevated level of an inflammatory marker suchas C-reactive protein). Reduction of a symptom can be recognizedsubjectively by the individual or an observer of the individual or canbe detected or identified by clinical and/or laboratory findings. Insome embodiments, compositions comprising an isolated form of a compoundof Formula I or IA (e.g., anatabine or S-(−)-anatabine) or a saltthereof are used to maintain inflammation at levels that promotewell-being.

Compounds of Formula I

In some embodiments, a composition comprises an isolated form of acompound of Formula I, which can be provided as a pharmaceuticallyacceptable or food-grade salt:

wherein:

-   -   R represents hydrogen or C₁-C₅ alkyl;    -   R′ represents hydrogen or C₁-C₇ alkyl; and    -   X represents halogen or C₁-C₇ alkyl.

In some embodiments,

-   -   R represents hydrogen or C₁-C₃ alkyl;    -   R′ represents hydrogen or C₁-C₄ alkyl; and    -   X represents halogen or C₁-C₃ alkyl.

The dotted line within the piperidine ring represents a carbon/carbon orcarbon/nitrogen double bond within that ring, or two conjugated doublebonds within that ring. One of the two conjugated double bonds can be acarbon/nitrogen double bond, or both of the conjugated double bonds canbe carbon/carbon double bonds. When a carbon/nitrogen double bond ispresent, R is absent; and either (i) “a” is an integer ranging from 1-4,usually 1-2, and “b” is an integer ranging from 0-8, usually 0-4; or(ii) “a” is an integer ranging from 0-4, usually 0-2, and “b” is aninteger ranging from 1-8, usually 1-4. When a carbon/nitrogen doublebond is not present, R is present; “a” is an integer ranging from 0-4,usually 1-2; and “b” is an integer ranging from 0-8, usually 0-4 or 1-2.The term “alkyl,” as used herein, encompasses both straight chain andbranched alkyl. The term “halogen” encompasses fluorine (F), chlorine(Cl), bromine (Br), and iodine (I).

Table 1 below illustrates non-limiting examples of compounds withinFormula I:

TABLE 1 R R′ (position) X (position) a b H CH₃ (3) — 0 1 CH₃ — CH₃ (5) 10 H — CH₃CH₂ (4) 1 0 CH₃CH₂ CH₃ (4) — 0 1 H CH₃ (2) — 0 2 CH₃CH₂ (5) HCH₃ (3) CH₃ (5) 1 1 CH₃ — CH₃ (2) 2 0 CH₃ (5)

Compounds of Formula I may be present in the form of racemic mixturesor, in some cases, as isolated enantiomers as illustrated below inFormulas IA and IB.

An example of a compound of Formula I is anatabine. An example of acompound of Formula IA is S-(−)-anatabine, and an example of compound ofFormula IB is R-(+)-anatabine.

The chemical structure of anatabine(1,2,3,6-tetrahydro-[2,3′]bipyridinyl) is illustrated below, in which *designates an asymmetric carbon.

Anatabine exists in tobacco and certain foods and plants, includinggreen tomatoes, green potatoes, ripe red peppers, tomatillos, sundriedtomatoes, datura, mandrake, belladonna, capsicum, eggplant, and petunia,as a mixture of R-(+)-anatabine and S-(−)-anatabine, whose structuresare illustrated below.

Anatabine, R-(+)-anatabine, S-(−)-anatabine, and other compounds ofFormula I can be prepared synthetically. Such synthetic preparationtechniques produce isolated forms of the compounds. Methods forselectively preparing the anatabine enantiomers are described, forexample, in “A General Procedure for the Enantioselective Synthesis ofthe Minor Tobacco Alkaloids Nornicotine, Anabasine, and Anatabine,” TheAAPS Journal 2005; 7(3) Article 75.

In some embodiments, anatabine is prepared via a benzophenoneiminepathway, as described in co-pending and commonly owned application Ser.No. 12/729,346, filed Mar. 23, 2010, the disclosure of which isincorporated herein by reference in its entirety.

Anatabine

In some embodiments, a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) may be adsorbed on a cation exchange resin such aspolymethacrilic acid (Amberlite IRP64 or Purolite C115HMR), as describedin U.S. Pat. No. 3,901,248, the disclosure of which is herebyincorporated by reference in its entirety. Such cation exchange resinshave been used commercially, for example, in nicotine replacementtherapy, e.g., nicotine polacrilex.

In some embodiments, a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) is provided in the form of a salt. “Salt,” as usedherein, includes pharmaceutically acceptable and food-grade salts. Ingeneral, salts may provide improved chemical purity, stability,solubility, and/or bioavailability relative to anatabine in its nativeform. Non-limiting examples of possible anatabine salts are described inP. H. Stahl et al., Handbook of Pharmaceutical Salts: Properties,Selection and Use, Weinheim/Zürich:Wiley-VCH/VHCA, 2002, including saltsof 1-hydroxy-2-naphthoic acid, 2,2-dichloroacetic acid,2-hydroxyethanesulfonic acid, 2-oxoglutaric acid, 4-acetamidobenzoicacid, 4-aminosalicylic acid, acetic acid, adipic acid, ascorbic acid(L), aspartic acid (L), benzenesulfonic acid, benzoic acid, camphoricacid (+), camphor-10-sulfonic acid (+), capric acid (decanoic acid),caproic acid (hexanoic acid), caprylic acid (octanoic acid), carbonicacid, cinnamic acid, citric acid, cyclamic acid, dodecylsulfuric acid,ethane-1,2-disulfonic acid, ethanesulfonic acid, formic acid, fumaricacid, galactaric acid, gentisic acid, glucoheptonic acid (D), gluconicacid (D), glucuronic acid (D), glutamic acid, glutaric acid,glycerophosphoric acid, glycolic acid, hippuric acid, hydrobromic acid,hydrochloric acid, isobutyric acid, lactic acid (DL), lactobionic acid,lauric acid, maleic acid, malic acid (−L), malonic acid, mandelic acid(DL), methanesulfonic acid, naphthalene-1,5-disulfonic acid,naphthalene-2-sulfonic acid, nicotinic acid, nitric acid, oleic acid,oxalic acid, palmitic acid, pamoic acid, phosphoric acid, proprionicacid, pyroglutamic acid (−L), salicylic acid, sebacic acid, stearicacid, succinic acid, sulfuric acid, tartaric acid (+L), thiocyanic acid,toluenesulfonic acid (p), and undecylenic acid.

As an alternative to preparing anatabine synthetically, anatabine can beobtained by extraction from tobacco or other plants, such as members ofthe Solanaceae family, such as datura, mandrake, belladonna, capsicum,potato, nicotiana, eggplant, and petunia. For example, a tobacco extractmay be prepared from cured tobacco stems, lamina, or both. In theextraction process, cured tobacco material is extracted with a solvent,typically water, ethanol, steam, or carbon dioxide. The resultingsolution contains the soluble components of the tobacco, includinganatabine. Anatabine may be purified from the other components of thetobacco using suitable techniques such as liquid chromatography.

As part of the purification process, tobacco material may besubstantially denicotinized to remove a majority of other alkaloids suchas nicotine, nornicotine, and anabasine. Denicotinizing is usuallycarried out prior to extraction of anatabine. Methods that may be usedfor denicotinizing tobacco materials are described, for example, in U.S.Pat. No. 5,119,835, the disclosure of which is hereby incorporated byreference. In general, tobacco alkaloids may be extracted from tobaccomaterial with carbon dioxide under supercritical conditions. The tobaccoalkaloids may then be separated from the carbon dioxide by dissolving anorganic acid or a salt thereof, such as potassium monocitrate, in thecarbon dioxide.

In some embodiments, an isolated form of anatabine is used. An “isolatedform of anatabine,” as used herein, refers to anatabine that either hasbeen prepared synthetically or has been substantially separated fromplant materials in which it occurs naturally. The isolated form ofanatabine should have a very high purity (including enantiomeric purityin the case where an enantiomer is used). In the case of syntheticanatabine, for example, purity refers to the ratio of the weight ofanatabine to the weight of the end reaction product. In the case ofisolating anatabine from plant material, for example, purity refers tothe ratio of the weight of anatabine to the total weight of theanatabine-containing extract. Usually, the level of purity is at leastabout 95%, more usually at least about 96%, about 97%, about 98%, orhigher. For example, the level of purity may be about 98.5%, 99.0%,99.1%, 99.2%, 99.3%, 99.4%, 99.5%, 99.6%, 99.7%, 99.8%, 99.9%, orhigher. Use of such isolated forms avoids the toxicity associated withtobacco, tobacco extracts, alkaloid extracts, and nicotine.

Anatabine and Inflammation

Without being bound by this explanation, data presented in Examplesbelow indicate that anatabine reduces transcription mediated by nuclearfactor KB (NFκB). NFκB is a transcription factor which operates in cellsinvolved in inflammatory and immune reactions. As documented in TableIA, NFκB-mediated transcription is associated with numerous disorders,including those with an inflammatory component, an aberrant immuneresponse, and/or inappropriate cell proliferation. Isolated forms of acompound of Formula I or IA (e.g., anatabine or S-(−)-anatabine) orsalts thereof are useful for treating disorders comprising an“NFκB-mediated inflammatory component,” i.e. inflammation characterizedby, caused by, resulting from, or affected by NFκB-mediatedtranscription.

NFκB-mediated transcription is implicated in an enormous variety ofmaladies. Based on anatabine's surprising efficacy in interfering withor interrupting this pivotal inflammatory-related activity, a compoundof Formula I or IA (e.g., anatabine or S-(−)-anatabine) can be expectedto have a wide range of therapeutic utilities. Unless otherwise clearfrom context, the term “anatabine” as used herein refers collectively toanatabine, either as a racemic mixture or an enantiomer, andpharmaceutically acceptable or food-grade salts of either of them.

Disorders

In some embodiments, an isolated form a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof can beadministered to reduce the risk of developing a disorder comprising anNFκB-mediated inflammatory component (i.e., prophylactically). One canreadily identify individuals with an increased risk or family history ofa disorder. Other recognized indices of elevated risk of certaindisorders can be determined by standard clinical tests or medicalhistory.

In some embodiments, the disorder is an immune or autoimmune disorder.In some embodiments, the disorder is thyroiditis. In some embodiments,the disorder is arthritis, such as rheumatoid arthritis, primary andsecondary osteoarthritis (also known as degenerative joint disease). Insome embodiments, the disorder is a spondyloarthropathy, such aspsoriatic arthritis, juvenile chronic arthritis with late pannus onset,and enterogenic spondyloarthropathies such as enterogenic reactivearthritis, urogenital spondyloarthropathy, and undifferentiatedspondyloarthropathy. In some embodiments, the disorder is a myopathy,such as “soft tissue rheumatism” (e.g., tennis elbow, frozen shoulder,carpal tunnel syndrome, plantar fasciitis, and Achilles tendonitis).

In some embodiments, the disorder is diabetes, either type I diabetes ortype II diabetes. In other embodiments the disorder is agastrointestinal inflammatory disorder, such as an inflammatory boweldisease. Examples of inflammatory bowel disease include, but are notlimited to, Crohn's disease, Barrett's syndrome, ileitis, irritablebowel syndrome, irritable colon syndrome, ulcerative colitis,pseudomembranous colitis, hemorrhagic colitis, hemolytic-uremic syndromecolitis, collagenous colitis, ischemic colitis, radiation colitis, drugand chemically induced colitis, diversion colitis, colitis in conditionssuch as chronic granulomatous disease, celiac disease, celiac sprue,food allergies, gastritis, infectious gastritis, enterocolitis (e.g.,Helicobacter pylori-infected chronic active gastritis), and pouchitis.

In other embodiments the disorder is graft-versus-host-disease (GVHD),systemic lupus erythematosus (SLE), lupus nephritis, Addison's disease,Myasthenia gravis, vasculitis (e.g., Wegener's granulomatosis),autoimmune hepatitis, osteoporosis, and some types of infertility.

In some embodiments, the disorder is vascular inflammatory disease,associated vascular pathologies, atherosclerosis, angiopathy,inflammation-induced atherosclerotic or thromboembolic macroangiopathy,coronary artery disease, cerebrovascular disease, peripheral vasculardisease, cardiovascular circulatory disease such asischemia/reperfusion, peripheral vascular disease, restenosis followingangioplasty, inflammatory aortic aneurysm, vasculitis, stroke, spinalcord injury, congestive heart failure, hemorrhagic shock, ischemic heartdisease/reperfusion injury, vasospasm following subarachnoid hemorrhage,vasospasm following cerebrovascular accident, pleuritis, pericarditis,inflammation-induced myocarditis, or a cardiovascular complication ofdiabetes.

In some embodiments, the disorder is brain swelling or aneurodegenerative disease such as multiple sclerosis, Alzheimer'sdisease, or Parkinson's disease. In other embodiments the disorder isinflammation related to a kidney disease, nephritis, glomerulonephritis,dialysis, peritoneal dialysis, pericarditis, chronic prostatitis,vasculitis, gout, or pancreatitis.

In some embodiments, the disorder is an anemia. In other embodiments thedisorder is an ulcer-related disease, such as peptic ulcer disease,acute pancreatitis, or aphthous ulcer. In other embodiments the disorderis related to an age-related disease, such as atherosclerosis, fibrosis,and osteoporosis, or a disorder associated with pre-maturity, such asretinopathy, chronic lung disease, arthritis, and digestive problems.

In other embodiments the disorder is preeclampsia, inflammation relatedto chemical or thermal trauma due to burns, acid, and alkali, chemicalpoisoning (MPTP/concavalin/chemical agent/pesticide poisoning), snake,spider, or other insect bites, adverse effects from drug therapy(including adverse effects from amphotericin B treatment), adverseeffects from immunosuppressive therapy (e.g., interleukin-2 treatment),adverse effects from OKT3 treatment, adverse effects from GM-CSFtreatment, adverse effects of cyclosporine treatment, and adverseeffects of aminoglycoside treatment, stomatitis and mucositis due toimmunosuppression, or exposure to ionizing radiation, such as solarultraviolet exposure, nuclear power plant or bomb exposure, or radiationtherapy exposure, such as for therapy for cancer.

In some embodiments, the disorder is a periodontal disease, such asplaque-associated gingivitis; acute necrotizing ulcerative gingivitis;hormone-induced gingival inflammation; drug-influenced gingivitis;linear gingival erythema (LGE); gingivitis due to bacterial, viral, orfungal infection; gingivitis due to blood dyscrasias or mucocutaneousdiseases (e.g., lichen planus, pemphigus vulgaris, and desquamativegingivitis); plaque-associated adult periodontitis; early-onsetperiodontitis; prepubertal periodontitis; juvenile periodontitis;rapidly progressive periodontitis; periodontitis associated withsystemic diseases; necrotizing ulcerative periodontitis; refractoryperiodontitis; and peri-implantitis.

In some embodiments, the disorder is a cancer, such as acutelymphoblastic leukemia, acute myeloid leukemia, adrenocorticalcarcinoma, AIDS-related lymphoma, anal cancer, appendix cancer, grade I(anaplastic) astrocytoma, grade II astrocytoma, grade III astrocytoma,grade IV astrocytoma, atypical teratoid/rhabdoid tumor of the centralnervous system, basal cell carcinoma, bladder cancer, breast cancer,breast sarcoma, bronchial cancer, bronchoalveolar carcinoma, Burkittlymphoma, cervical cancer, chronic lymphocytic leukemia, chronicmyelogenous leukemia, colon cancer, colorectal cancer,craniopharyngioma, cutaneous T-cell lymphoma, endometrial cancer,endometrial uterine cancer, ependymoblastoma, ependymoma, esophagealcancer, esthesioneuroblastoma, Ewing's sarcoma, extracranial germ celltumor, extragonadal germ cell tumor, extrahepatic bile duct cancer,fibrous histiocytoma, gallbladder cancer, gastric cancer,gastrointestinal carcinoid tumor, gastrointestinal stromal tumor,gestational trophoblastic tumor, gestational trophoblastic tumor,glioma, hairy cell leukemia, head and neck cancer, heart cancer,hepatocellular cancer, Hilar cholangiocarcinoma, Hodgkin's lymphoma,hypopharyngeal cancer, intraocular melanoma, islet cell tumor, Kaposisarcoma, Langerhans cell histiocytosis, large-cell undifferentiated lungcarcinoma, laryngeal cancer, lip cancer, lung adenocarcinoma, lymphoma,macroglobulinemia, malignant fibrous histiocytoma, medulloblastoma,medulloepithelioma, melanoma, Merkel cell carcinoma, mesothelioma,endocrine neoplasia, multiple myeloma, mycosis fungoides,myelodysplasia, myelodysplastic/myeloproliferative neoplasms,myeloproliferative disorders, nasal cavity cancer, nasopharyngealcancer, neuroblastoma, non-Hodgkin's lymphoma, oral cancer,oropharyngeal cancer, osteosarcoma, ovarian clear cell carcinoma,ovarian epithelial cancer, ovarian germ cell tumor, pancreatic cancer,papillomatosis, paranasal sinus cancer, parathyroid cancer, penilecancer, pharyngeal cancer, pineal parenchymal tumor, pineoblastoma,pituitary tumor, plasma cell neoplasm, plasma cell neoplasm,pleuropulmonary blastoma, primary central nervous system lymphoma,prostate cancer, rectal cancer, renal cell cancer, respiratory tractcancer with chromosome 15 changes, retinoblastoma, rhabdomyosarcoma,salivary gland cancer, Sézary syndrome, small cell lung cancer, smallintestine cancer, soft tissue sarcoma, squamous cell carcinoma, squamousnon-small cell lung cancer, squamous neck cancer, supratentorialprimitive neuroectodermal tumor, supratentorial primitiveneuroectodermal tumor, testicular cancer, throat cancer, thymiccarcinoma, thymoma, thyroid cancer, cancer of the renal pelvis, urethralcancer, uterine sarcoma, vaginal cancer, vulvar cancer, Waldenströmmacroglobulinemia, or Wilms tumor.

In some embodiments, the disorder is an upper respiratory tractinfections (URI or URTI), such as tonsillitis, pharyngitis, laryngitis,sinusitis, otitis media, and the common cold. Infections which can betreated include, but are not limited to, rhinitis (e.g., inflammation ofthe nasal mucosa); rhinosinusitis or sinusitis (e.g., inflammation ofthe nares and paranasal sinuses, including frontal, ethmoid, maxillary,and sphenoid sinuses); nasopharyngitis (rhinopharyngitis or the commoncold; e.g., inflammation of the nares, pharynx, hypopharynx, uvula, andtonsils); pharyngitis (e.g., inflammation of the pharynx, hypopharynx,uvula, and tonsils); epiglottitis (supraglottitis; e.g., inflammation ofthe superior portion of the larynx and supraglottic area); laryngitis(e.g., inflammation of the larynx); laryngotracheitis (e.g.,inflammation of the larynx, trachea, and subglottic area); andtracheitis (e.g., inflammation of the trachea and subglottic area). Byreducing underlying inflammation, symptoms which can be treated include,but are not limited to, cough, sore throat, runny nose, nasalcongestion, headache, low grade fever, facial pressure, and sneezing.

In some embodiments, the disorder is a seizure disorder, i.e., anycondition characterized by seizures, described in more detail below.Neuroinflammation is a well-established response to central nervoussystem injury (Minghetti, Curr Opin Neurol 2005; 18:315-21). Humanpathologic, in vitro, and in vivo studies of Alzheimer's disease haveimplicated a glia-mediated neuroinflammatory response both in thepathophysiology of the disease (Mrak & Griffin, Neurobiol Aging26:349-54, 2005) and as treatment target (Hu et al., Bioorgan Med ChemLett 17:414-18, 2007; Ralay et al., J Neurosci 26:662-70, 2006; Craft etal., Exp Opin Therap Targets 9:887-900, 2005). Microglial activationleading to overexpression of IL-1 has been proposed as the pivotal stepin initiating a self propagating cytokine cycle culminating inneurodegeneration (Mrak & Griffin, Neurobiol Aging 26:349-54, 2005;Sheng et al., Neurobiol Aging 17:761-66, 1996). As noted above, datapresented in Examples 1 and 2 below indicate that anatabine reducestranscription mediated by nuclear factor κB (NFκB). IL-1β andpro-inflammatory cytokines may also function in epilepsy aspro-convulsant signaling molecules independent of such a cycle (Vezzaniet al., Epilepsia 43:S30-S35, 2002), which provides a potentialtherapeutic target in epilepsy and other seizure disorders (Vezzani &Granata, Epilepsia 46:1724-43, 2005).

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto treat seizures, including the generalized and partial seizures. Asdescribed in The Pharmacological Basis of Therapeutics, 9^(th) ed.,(McGraw-Hill), there are two classes of seizures: partial seizures andgeneralized seizures. Partial seizures consist of focal and localseizures. Partial seizures are further classified as simple partialseizures, complex partial seizures and partial seizures secondarilygeneralized. Generalized seizures are classified as convulsive andnonconvulsive seizures. They are further classified as absence(previously referred to as ‘petit mal’) seizures, atypical absenceseizures, myoclonic seizures, clonic seizures, tonic seizures,tonic-clonic seizures, and atonic seizures.

Generalized seizures include infantile spasms, absence seizures,tonic-clonic seizures, atonic seizures, and myoclonic seizures. Abnormalmotor function and a loss of consciousness are major features of theseseizures. A patient may also experience an aura of sensory, autonomic,or psychic sensations. The aura may include paresthesia, a risingepigastric sensation, an abnormal smell, a sensation of fear, or a dejavu sensation. A generalized seizure is often followed by a postictalstate, in which a patient may sleep deeply, be confused, and/or have aheadache or muscle ache. Todd's paralysis (limb weakness contralateralto the seizure focus) may be present in the postictal state.

Infantile spasms are characterized by frequent flexion and adduction ofthe arms and forward flexion of the trunk, usually of short duration.They occur only in the first 5 years of life.

Typical absence seizures (also known as petit mal seizures) arecharacterized by a loss of consciousness with eyelid fluttering,typically for 10-30 seconds or more. There may or may not be a loss ofaxial muscle tone. Convulsions are absent; instead, patients abruptlystop activity, then abruptly resume it, often without realizing that aseizure has occurred. Absence seizures are genetic. They occurpredominantly in children, often frequently throughout the day.

Atypical absence seizures occur as part of the Lennox-Gastaut syndrome,a severe form of epilepsy. They last longer than typical absenceseizures and jerking or automatic movements are more pronounced.

Atonic seizures occur most often in children, usually as part ofLennox-Gastaut syndrome. They are characterized by a complete loss ofmuscle tone and consciousness.

Tonic seizures also occur most often in children, usually as part ofLennox-Gastaut syndrome. They are characterized by tonic (sustained)contraction of axial and proximal muscles, usually during sleep, andlast 10 to 15 seconds. In longer tonic seizures a few, rapid clonicjerks may occur at the end of the seizure.

Tonic-clonic seizures, also known as grand mal seizures, may beprimarily or secondarily generalized. A patient experiencing a primarilygeneralized tonic-clonic seizure will often cry out, then loseconsciousness and fall. Tonic contractions then begin, followed byclonic (rapidly alternating contraction and relaxation) motion ofmuscles of the extremities, trunk, and head. A patient may lose urinaryand fecal continence, bite his tongue, and froth at the mouth. Seizuresusually last 1 to 2 min. There is no aura. Secondarily generalizedtonic-clonic seizures begin with a simple partial or complex partialseizure, and then progress to a generalized seizure.

Myoclonic seizures are characterized by brief, rapid jerks of a limb,several limbs, or the trunk. They may be repetitive, leading to atonic-clonic seizure. The jerks may be bilateral or unilateral.Consciousness is not lost unless the seizures progress into ageneralized tonic-clonic seizure.

Juvenile myoclonic epilepsy is an epilepsy syndrome characterized bymyoclonic, tonic-clonic, and absence seizures. Patients are usuallyadolescents. Seizures typically begin with bilateral, synchronousmyoclonic jerks, followed in 90% by generalized tonic-clonic seizures.They often occur on rising in the morning. A third of patients mayexperience absence seizures.

Febrile seizures are associated with fever, but not intracranialinfection. Benign febrile seizures are characterized by generalizedtonic-clonic seizures of brief duration. Such seizures are common inchildren, affecting up to four percent of children younger than sixyears of age. Complicated febrile seizures are characterized by focalseizures lasting more than fifteen minutes or occurring more than twicein twenty four hours. Two percent of children with febrile seizuresdevelop a subsequent seizure disorder. The risk is greater in childrenwith complicated febrile seizures, preexisting neurologic abnormalities,onset before age 1 year, or a family history of seizure disorders.

Status epilepticus is a seizure disorder characterized by tonic-clonicseizure activity lasting more than five to ten minutes, or two or moreseizures between which patients do not fully regain consciousness. Ifuntreated, seizures lasting more than sixty minutes may cause braindamage or death.

Complex partial status epilepticus and absence status epilepticus arecharacterized by prolonged episodes of mental status changes.Generalized convulsive status epilepticus may be associated with abruptwithdrawal of anticonvulsants or head trauma.

Simple partial seizures are characterized by motor, sensory, orpsychomotor symptoms without loss of consciousness. Seizures indifferent parts of the brain often produce distinct symptoms.

An aura often precedes complex partial seizures. Patients are usuallyaware of their environment but may experience impaired consciousness.Patients may also experience oral automatisms (involuntary chewing orlip smacking), hand or limb automatisms (automatic purposelessmovements), utterance of unintelligible sounds, tonic or dystonicposturing of the extremity contralateral to the seizure focus, head andeye deviation, usually in a direction contralateral to the seizurefocus, and bicycling or pedaling movements of the legs, especially wherethe seizure emanates from the medial frontal or orbitofrontal headregions. Motor symptoms subside after one or two minutes, and confusionand disorientation one to two minutes later. Postictal amnesia iscommon.

Epilepsy is an important example of a seizure disorder. “Epilepsy”describes a group of central nervous system disorders that arecharacterized by recurrent seizures that are the outward manifestationof excessive and/or hyper-synchronous abnormal electrical activity ofneurons of the cerebral cortex and other regions of the brain. Thisabnormal electrical activity can be manifested as motor, convulsion,sensory, autonomic, or psychic symptoms.

Hundreds of epileptic syndromes have been defined as disorderscharacterized by specific symptoms that include epileptic seizures.These include, but are not limited to, absence epilepsy, psychomotorepilepsy, temporal lobe epilepsy, frontal lobe epilepsy, occipital lobeepilepsy, parietal lobe epilepsy, Lennox-Gastaut syndrome, Rasmussen'sencephalitis, childhood absence epilepsy, Ramsay Hunt Syndrome type II,benign epilepsy syndrome, benign infantile encephalopathy, benignneonatal convulsions, early myoclonic encephalopathy, progressiveepilepsy and infantile epilepsy. A patient may suffer from anycombination of different types of seizures. Partial seizures are themost common, and account for approximately 60% of all seizure types.

Hence, examples of generalized seizures which may be treated includeinfantile spasms, typical absence seizures, atypical absence seizures,atonic seizures, tonic seizures, tonic-clonic seizures, myoclonicseizures, and febrile seizures. Examples of partial seizures which maybe treated include simple partial seizures affecting the frontal lobe,contralateral frontal lobe, supplementary motor cortex, the insula, theInsular-orbital-frontal cortex, the anteromedial temporal lobe, theamygdala (including the opercular and/or other regions), the temporallobe, the posterior temporal lobe, the amygdala, the hippocampus, theparietal lobe (including the sensory cortex and/or other regions), theoccipital lobe, and/or other regions of the brain.

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto treat an epileptic syndrome including, but not limited to, absenceepilepsy, psychomotor epilepsy, temporal lobe epilepsy, frontal lobeepilepsy, occipital lobe epilepsy, parietal lobe epilepsy,Lennox-Gastaut syndrome, Rasmussen's encephalitis, childhood absenceepilepsy, Ramsay Hunt Syndrome type II, benign epilepsy syndrome, benigninfantile encephalopathy, benign neonatal convulsions, early myoclonicencephalopathy, progressive epilepsy and infantile epilepsy.

An isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof may also be useful for treating theaura that accompanies seizures. Thus, impaired consciousness, oralautomatisms, hand or limb automatisms, utterance of unintelligiblesounds, tonic or dystonic posturing of extremities, head and eyedeviation, bicycling or pedaling movements of the legs and othersymptoms that comprise the aura also may be treated.

Patients who can be treated include adults, teenagers, children, andneonates. Neonatal seizures are associated with later neurodevelopmentaland cognitive deficits including mental retardation, autism, andepilepsy, and it is estimated that up to 40% of cases of autism sufferfrom epilepsy or have a history of or seizures earlier in life.Accordingly, important target patients are infants, particularlyneonates, and persons with a personal or family a history of seizure,mental retardation or autism.

This disclosure also provides methods and compositions for treating apatient post-seizure. In one embodiment, an isolated form of a compoundof Formula I or IA (e.g., anatabine or S-(−)-anatabine) or a saltthereof is administered in conjunction with a second therapeutic agent,such as a neurotransmitter receptor inhibitor (e.g., an inhibitor of anAMPA receptor, NMDA receptor GABA receptor, chloride cotransporters, ormetabatropic glutamate receptor), a kinase/phosphatase inhibitor (e.g.,an inhibitor of calmodulin kinase II (CamK II), protein kinase A (PKA),protein kinase C (PKC), MAP Kinase, Src kinase, ERK kinase or thephosphatase calcineurin), and/or a protein translation inhibitor.

Calmodulin kinase II (CamK II) inhibitors include KN-62, W-7, HA-1004,HA-1077, and staurosporine. Protein kinase A (PKA) inhibitors includeH-89, HA-1004, H-7, H-8, HA-100, PKI, and staurosporine.

Protein kinase C (PKC) inhibitors include competitive inhibitors for thePKC ATP-binding site, including staurosporine and itsbisindolylmaleimide derivatives, Ro-31-7549, Ro-31-8220, Ro-31-8425,Ro-32-0432 and Sangivamycin; drugs which interact with the PKC'sregulatory domain by competing at the binding sites of diacylglyceroland phorbol esters, such as calphostin C, Safingol,D-erythro-Sphingosine; drugs which target the catalytic domain of PKC,such as chelerythrine chloride, and Melittin; drugs which inhibit PKC bycovalently binding to PKC upon exposure to UV lights, such asdequalinium chloride; drugs which specifically inhibit Ca-dependent PKCsuch as Go6976, Go6983, Go7874 and other homologs, polymyxin B sulfate;drugs comprising competitive peptides derived from PKC sequence; and[0056]PKC inhibitors such as cardiotoxins, ellagic acid, HBDDE,1-O-Hexadecyl-2-O-methyl-rac-glycerol, Hypercin, K-252, NGIC-I,Phloretin, piceatannol, and Tamoxifen citrate.

MAP kinase inhibitors include SB202190 and SB203580. SRC kinaseinhibitors include PP1, PP2, Src Inhibitor No. 5, SU6656, andstaurosporine. ERK kinase inhibitors include PD 98059, SL327,olomoucine, and 5-Iodotubercidin. Calcineurin inhibitors includetacrolimus and cyclosporine.

Protein translation inhibitors include mTOR inhibitors, such asrapamycin, CCI-779 and RAD 001.

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) is administered to treat an AutismSpectrum Disorder. Autism spectrum disorders (ASDs) are pervasiveneurodevelopmental disorders diagnosed in early childhood when acquiredskills are lost or the acquisition of new skills becomes delayed. ASDsonset in early childhood and are associated with varying degrees ofdysfunctional communication and social skills, in addition to repetitiveand stereotypic behaviors. In many cases (25%-50%), a period ofseemingly normal development drastically shifts directions as acquiredskills are lost or the acquisition of new skills becomes delayed.Examples of Autism Spectrum Disorders include “classical” autism,Asperger's syndrome, Rett syndrome, childhood disintegrative disorder,and atypical autism otherwise known as pervasive developmental disordernot otherwise specified (PDD-NOS).

Autism is a childhood psychosis originating in infancy and characterizedby a wide spectrum of psychological symptoms that progress with age(e.g., lack of responsiveness in social relationships, languageabnormality, and a need for constant environmental input). It generallyappears in children between the ages of two and three years and givesrise to a loss of the development previously gained by the child.Autistic individuals are at increased risk of developing seizuredisorders, such as epilepsy.

Excess inflammation has been found in the colon, esophagus, and duodenumof patients with autism, and postmortem studies have also shown anincrease in the expression of several markers for neuroinflammation(e.g., Wakefield et al., Lancet 351, 351-52, 1998; Wakefield et al.,Lancet 351, 637-41, 1998; and Vargas et al., Ann Neurol 57, 67-81,2004). Proinflammatory cytokines, including TNFα and IL-1, areoverproduced in a subset of autistic patients, indicating that thesepatients had excessive innate immune responses and/or aberrantproduction of regulatory cytokines for T cell responses (e.g.,20030148955. Isolated forms of compounds of Formula I or IA (e.g.,anatabine or S-(−)-anatabine) or salts thereof are particularly usefulfor treating disorders comprising an “NFκB-mediated inflammatorycomponent,” i.e. inflammation characterized by, caused by, resultingfrom, or affected by NFκB-mediated transcription. Thus, a compound ofFormula I or IA (e.g., anatabine or S-(−)-anatabine) in isolated formmay be useful in treating or reducing a symptom of an ASD.

In some embodiments, the dose sufficient to reduce a symptom of thedisorder can include a series of treatments. For example, an individualcan be treated with a dose of an isolated form of anatabine orS-(−)-anatabine or a salt thereof several times per day (e.g., 2-12 or4-10 times per day), once daily, or less frequently such as 1-6 timesper week.

In some embodiments, the compound administered is an isolated form of acompound of Formula I or IA (e.g., anatabine or S-(−)-anatabine) whichis administered several times per day (e.g., 2-12 or 4-10 times perday), once daily, or less frequently such as 1-6 times per week.Treatments may span between about 1 to 10 weeks (e.g., between 2 to 8weeks, between 3 to 7 weeks, for about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10weeks). It will also be appreciated that a dose regimen used fortreatment may increase or decrease over the course of a particulartreatment.

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof can beadministered to reduce the risk of developing an ASD (i.e.,prophylactically). One can readily identify individuals with anincreased risk or family history of a disorder. Other recognized indicesof elevated risk of certain disorders can be determined by standardclinical tests or medical history.

An isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof can also be used to improve erectiledysfunction, either administered alone of in conjunction with othertherapies such as tadalafil (e.g. CIALIS®), vardenafil (e.g., LEVITRA®,STAXYN®), and sildenafil (e.g., VIAGRA®).

In some embodiments, a therapeutically effective dose of an isolatedform of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof can be administered to an individualfor treating alopecia areata or other disorders associated with hairloss.

Doses

In some embodiments an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto an individual in an amount sufficient to reduce NFκB-mediatedtranscription (“NFκB-inhibiting amounts”). In some embodiments, anisolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof is administered to an individual at adose sufficient to reduce a symptom of a disorder with anNFκB-mediated-transcription component, such as the disorders describedabove. “Individual” as used herein includes warm-blooded animals,typically mammals, including humans and other primates. In someembodiments, the individual is an animal such as a companion animal, aservice animal, a farm animal, or a zoo animal. Such animals include,but are not limited to, canines (including dogs, wolves), felines(including domestic cats, tigers, lions), ferrets, rabbits, rodents(e.g., rats, mice), guinea pigs, hamsters, gerbils, horses, cows, pigs,sheep, goats, giraffes, and elephants. In some embodiments, theindividual is a non-human mammal.

In some embodiments an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto an individual to treat a disorder comprising an inflammatorycomponent or a symptom of such a disorder. In some embodiments theinflammatory component is chronic, low-level inflammation. In someembodiments the symptom is eliminated. In some embodiments the symptomis reduced in frequency, severity, or duration. In some embodiments theonset of the symptom is delayed.

In some embodiments an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto an individual before manifestation of a symptom. In some embodimentsthe symptom is a subjective indication. In some embodiments the symptomis an objective indication. In some embodiments, the symptom is anelevated level of an inflammatory marker such as C-reactive protein.

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is administeredto an individual after manifestation of a symptom. In some embodimentsthe symptom is a subjective indication. In some embodiments the symptomis an objective indication. In some embodiments, the symptom is anelevated level of an inflammatory marker such as C-reactive protein.

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or a salt thereof is used tomaintain inflammation at levels that promote well-being.

Daily doses typically range from about 1 μg/kg to about 7 mg/kg bodyweight, e.g.:

-   -   i. about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1,        2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4,        3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7,        4.8, 4.9, or 5 μg/kg;    -   ii. about 0.1, 0.11, 0.12, 0.125, 0.13, 0.14, 0.145, 0.15, 0.16,        0.17, 0.175, 0.18, 0.19, 0.2, 0.3, 0.31, 0.32, 0.33, 0.34, 0.35,        0.36, 0.37, 0.38, 0.39, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1,        1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4,        2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7,        3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, or 5        mg/kg);    -   iii. about 1.5 μg/kg to about 5 μg/kg, about 1 μg/kg to about 10        μg/kg, about 0.01 mg/kg to about 7 mg/kg body weight, about 0.1        mg/kg to about 5 mg/kg;    -   iv. about 0.1 mg/kg to about 2 mg/kg, about 1 mg/kg to about 3        mg/kg, about 0.5 mg/kg to about 2 mg/kg, about 1 mg/kg to about        2 mg/kg, about 3 mg/kg to about 5 mg/kg, about 2 mg/kg to about        4 mg/kg, about 2 mg/kg to about 5 mg/kg, or about 0.5 mg/kg to        about 1.5 mg/kg;    -   v. about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70,        71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 85, 90, 100, 105, 110,        115, 117, 118, 119, 120, 125, 130, 135, 136, 140, 145, 146, 147,        148, 149, 150, 175, 200, or 205 mg/kg; or    -   vi. about 55 to about 120 μg/kg, about 100 to about 150 μg/kg,        about 100 to about 200 μg/kg, about 110 to about 146 μg/kg,        about 118 to about 150 μg/kg, about 110 to about 150 μg/kg,        about 117 to about 147 μg/kg, about 70 to about 140 μg/kg, or        about 125 to about 350 140 μg/kg.

Dosages described above may apply to any of the disorders disclosedherein; however, certain factors may influence the dose sufficient toreduce a symptom of a disorder (i.e., an effective dose), including thetype and/or severity of the disease or disorder, previous treatments,the general health, age, and/or weight of the individual, the frequencyof treatments, the rate of release from the composition, and otherdiseases present. This dose may vary according to factors such as thedisease state, age, and weight of the subject. For example, higher dosesmay be administered for treatments involving conditions which are at anadvanced stage and/or life-threatening. Dosage regimens also may beadjusted to provide the optimum therapeutic response.

For example, in some embodiments, a neurodegenerative disease, such asAlzheimer's disease or Parkinson's disease, is treated by administeringan isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) in an amount that exceeds 150 μg per kg patient weight.In other embodiments, a neurodegenerative disease, such as Alzheimer'sdisease or Parkinson's disease, is treated by administering an isolatedform of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) in an amount that is between about 50 μg and 100 μg orbetween about 100 μg and 150 μg per kg patient weight.

In some embodiments, tablets comprising about 600 μg S-(−)-anatabinecitrate or about 1 mg anatabine citrate are administered from once to 25times daily (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15,16, 17, 18, 19, 20, 21, 22, 23, 24, or 25) times daily.

In some embodiments, thyroiditis is treated by administering to anindividual 600 μg anatabine citrate, 20 times daily over a period of 30days. In some embodiments, the individual is treated with approximately0.1 mg/kg/day of anatabine or S-(−)-anatabine.

In some embodiments, the dose sufficient to reduce the symptom of thedisorder being treated can include a series of treatments. For example,an individual can be treated with a dose of an isolated form of acompound of Formula I or IA (e.g., anatabine or S-(−)-anatabine) or asalt thereof several times per day (e.g., 2-12 or 4-10 times per day),once daily, or less frequently such as 1-6 times per week. Treatmentsmay span between about 1 to 10 weeks (e.g., between 2 to 8 weeks,between 3 to 7 weeks, for about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 weeks).It will also be appreciated that a dose regimen used for treatment mayincrease or decrease over the course of a particular treatment.

Use with Other Therapies

An isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or a salt thereof can be used in conjunction with(i.e., before, after, or at the same time as) other therapies for anydisorder with an NFκB-mediated component. In some embodiments, thesetherapies include other products that inhibit production ofNFκB-mediated inflammatory species. These products include, but are notlimited to, dexamethasone, glucocorticoids (e.g., prednisone, methylprednisolone), cyclosporine, tacrolimus, deoxyspergualin, non-steroidalantiinflammatory drugs (NSAIDs) such as aspirin and other salicylates,tepoxalin, synthetic peptide proteosome inhibitors, antioxidants (e.g.,N-acetyl-L-cysteine, vitamin A, vitamin C, vitamin E, dithiocarbamatederivatives, curcumin), IL-10, nitric oxide, cAMP, gold-containingcompounds, and gliotoxin.

Pharmaceutical Compositions

Pharmaceutical compositions may be formulated together with one or moreacceptable pharmaceutical or food grade carriers or excipients. As usedherein, the term “acceptable pharmaceutical or food grade carrier orexcipient” means a non-toxic, inert solid, semisolid or liquid filler,diluent, encapsulating material or formulation auxiliary of any type.For example, sugars such as lactose, glucose and sucrose; starches suchas corn starch and potato starch; cellulose and its derivatives such assodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate;powdered tragacanth; malt; gelatin; talc; excipients such as cocoabutter and suppository waxes; oils such as peanut oil, cottonseed oil,safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycolssuch as propylene glycol; esters such as ethyl oleate and ethyl laurate;agar; buffering agents such as magnesium hydroxide and aluminumhydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer'ssolution; ethyl alcohol, and phosphate buffer solutions, as well ascompatible lubricants such as sodium lauryl sulfate and magnesiumstearate, as well as coloring agents, releasing agents, coating agents,sweetening, flavoring and perfuming agents, preservatives andantioxidants can also be present in the composition, according to thejudgment of the formulator.

Pharmaceutical compositions may be prepared by any suitable techniqueand is not limited by any particular method for its production. Forexample, a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) can be combined with excipients and a binder, and thengranulated. The granulation can be dry-blended with any remainingingredients, and compressed into a solid form such as a tablet.

Pharmaceutical compositions may be administered by any suitable route.For example, the compositions may be administered orally, parenterally,by inhalation spray, topically, rectally, nasally, buccally, vaginally,via an implanted reservoir, or ingested as a dietary supplement or food.In some embodiments, a composition is provided in an inhaler, which maybe actuated to administer a vaporized medium that is inhaled into thelungs. The term parenteral as used herein includes subcutaneous,intracutaneous, intravenous, intramuscular, and intracranial injectionor infusion techniques. Most often, the pharmaceutical compositions arereadily administered orally and ingested.

Pharmaceutical compositions may contain any conventional non-toxicpharmaceutically-acceptable carriers, adjuvants or vehicles. In somecases, the pH of the formulation may be adjusted with acceptablepharmaceutical or food grade acids, bases or buffers to enhance thestability of the formulated composition or its delivery form.

Liquid dosage forms for oral administration include acceptablepharmaceutical or food grade emulsions, microemulsions, solutions,suspensions, syrups and elixirs. In addition to the active compounds,the liquid dosage forms may contain inert diluents commonly used in theart such as, for example, water or other solvents, solubilizing agentsand emulsifiers such as ethyl alcohol, isopropyl alcohol, ethylcarbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propyleneglycol, 1,3-butylene glycol, dimethylsulfoxide (DMSO) dimethylformamide,oils (in particular, cottonseed, groundnut, corn, germ, olive, castor,and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethyleneglycols and fatty acid esters of sorbitan, and mixtures thereof. Besidesinert diluents, the oral compositions can also include adjuvants such aswetting agents, emulsifying and suspending agents, sweetening,flavoring, and perfuming agents.

Solid dosage forms for oral administration include capsules, tablets,lozenges, pills, powders, and granules. In such solid dosage forms, theactive compound is mixed with at least one inert, acceptablepharmaceutical or food grade excipient or carrier such as sodium citrateor dicalcium phosphate and/or a) fillers or extenders such as starches,lactose, sucrose, glucose, mannitol, and silicic acid, b) binders suchas carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidone,sucrose and acacia, c) humectants such as glycerol, d) disintegratingagents such as agaragar, calcium carbonate, potato or tapioca starch,alginic acid, certain silicates, and sodium carbonate, e) solutionretarding agents such as paraffin, f) absorption accelerators such asquaternary ammonium compounds, g) wetting agents such as cetyl alcoholand glycerol monostearate, h) absorbents such as kaolin and bentoniteclay, i) lubricants such as talc, calcium stearate, magnesium stearate,solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof,and j) sweetening, flavoring, perfuming agents, and mixtures thereof. Inthe case of capsules, lozenges, tablets and pills, the dosage form mayalso comprise buffering agents.

The solid dosage forms of tablets, capsules, pills, and granules can beprepared with coatings and shells such as enteric coatings and othercoatings well known in the pharmaceutical formulating art. They mayoptionally contain opacifying agents and can also be of a compositionthat they release the active ingredient(s) only, or preferentially, in acertain part of the intestinal tract or, optionally, in a delayed orextended manner. Examples of embedding compositions which can be usedinclude polymeric substances and waxes. Tablet formulations for extendedrelease are also described in U.S. Pat. No. 5,942,244.

Inflammatory Markers

An isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) can be used to reduce elevated blood levels ofinflammatory markers such as CRP or to maintain healthy levels of suchmarkers. Thus, in some embodiments levels of inflammatory markers can beused to aid in determining doses of an isolated form of a compound ofFormula I or IA (e.g., anatabine or S-(−)-anatabine) to be administeredas well as to monitor treatment of various inflammatory disorders and toassist physicians in deciding on a course of a treatment for anindividual at risk of an inflammatory disorder. These markers include,but are not limited to, C-reactive protein (CRP), soluble intercellularadhesion molecule (sICAM-1), ICAM 3, BL-CAM, LFA-2, VCAM-1, NCAM, PECAM;fibrinogen, serum amyloid A (SAA), TNFα, lipoprotein associatedphospholipase A2 (LpPlA2), sCD40 ligand, myeloperoxidase, interleukin-6(IL-6), and interleukin-8 (IL-8).

The level of one or more inflammatory markers can be determined in apatient already being treated with an isolated form of a compound ofFormula I or IA (e.g., anatabine or S-(−)-anatabine) or in an individualat risk for an inflammatory disorder or suspected of having aninflammatory disorder. The level is compared to a predetermined value,and the difference indicates whether the patient will benefit fromadministration of an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or from continued administration ofan isolated form of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine). The level of inflammatory marker can be determined byany art recognized method. Typically, the level is determined bymeasuring the level of the marker in a body fluid, for example, blood,lymph, saliva, or urine. The level can be determined by ELISA, orimmunoassays or other conventional techniques for determining thepresence of the marker. Conventional methods include sending a sample(s)of a patient's body fluid to a commercial laboratory for measurement.

The predetermined value can take a variety of forms and will varyaccording to the inflammatory marker. The predetermined value can besingle cut-off value, such as a median or a mean, or it can be a range.The predetermined value also can depend on the individual or particularinflammatory disorder. Appropriate ranges and categories can be selectedby those of ordinary skill in the art using routine methods. See US2006/0115903; US 2004/0175754.

Markers such as CRP, sICAM-1, ICAM 3, BL-CAM, LFA-2, VCAM-1, NCAM,PECAM, fibrinogen, SAA, TNFα, lipoprotein associated phospholipase A2(LpPlA2), sCD40 ligand, myeloperoxidase, IL-6, and IL-8 are usefulmarkers for systemic inflammation. In some embodiments, the inflammatorymarker is CRP, which is associated both with cardiovascular disease (seeUS 2006/0115903) and cancer, such as colon cancer (Baron et al., N.Engl. J. Med. 348, 891-99, 2003). Elevated levels of CRP are alsoobserved in patients with insulin-resistance (Visser et al., JAMA. 1999,282(22):2131-5). Diabetic and insulin-resistant patients also haveelevated levels of TNFα, IL-6, and IL-8 (Roytblat et al., Obes Res.2000, 8(9):673-5; Straczkowski et al., J Clin Endocrinol Metab. 2002,87(10):4602-6; Hotamisligil et al., Science. 1996, 271(5249):665-8;Sartipy P, Loskutoff D J. Proc Natl Acad Sci USA. 2003, 100(12):7265-70;Hotamisligil et al., J Clin Invest. 1995, 95(5):2409-15).

Products Containing Anatabine

In addition to pharmaceutical compositions described above, isolatedforms of a compound of Formula I or IA (e.g., anatabine orS-(−)-anatabine) or salts thereof can be provided together with otheringredients, for example, in the form of an elixir, a beverage, a chew,a tablet, a lozenge, a gum, and the like.

In some embodiments a beverage suitable for human consumption contains aliquid medium and one or more isolated forms of a compound of Formula Ior IA (e.g., anatabine or S-(−)-anatabine) or salts thereof. The liquidmedium may be, for example, water of sufficiently high purity, or otherbeverage medium such as citrus juice or the like. The liquid medium andcompound(s) of Formula I or IA (e.g., anatabine or S-(−)-anatabine) orsalts thereof, may be combined with other ingredients to improve productcharacteristics, such as flavor, taste, color/clarity, and/or stability.Other beneficial components also may be added, such as vitamins,proteinaceous ingredients, or the like.

The components may be combined using appropriate equipment, such asblenders, and packaged in conventional beverage containers, such assingle-serving (or larger) glass bottles, plastic bottles, cans, or thelike. A beverage container may contain, for example, from about 100 mlto about 2,000 ml purified water and from about 0.00001 to about 0.0001wt % of an isolated form of a compound of Formula I or IA (e.g.,anatabine or S-(−)-anatabine) or a salt of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine).

In some embodiments, an isolated form of a compound of Formula I or IA(e.g., anatabine or S-(−)-anatabine) or salts thereof is provided in afluid form (e.g., a liquid, paste, cream, lotion, etc.) for topicalapplication. In some embodiments, the fluid form is a therapeuticproduct for use in treating dermatological disorders (e.g., psosriasis).In some embodiments, the fluid form is a skin care product such as amoisturizer or sunscreen. In some embodiments, the fluid form is acosmetic product. In some embodiments the fluid form is a toothpaste ora mouthwash.

The following examples illustrate but do not limit the scope of thedisclosure set forth above.

EXAMPLE 1 NFκB-Mediated Transcription Assays Cytotoxicity Assays

The effect of a range of doses of anatabine, nicotine, crude extract ofsmokeless tobacco, and alkaloid extract of smokeless tobacco wasexamined in an NFκB luciferase assay (inhibition of TNFα-induced NFκBactivity). The smokeless tobacco used in these experiments was plainlong-leaf Copenhagen tobacco purchased from a local vendor. Crudeextract was extracted with methanol and water and clarified bycentrifugation and filtration. The alkaloid extract was prepared fromsodium hydroxide and methanol extraction, organic phase separation andpurification. All treatment samples were prepared as a function ofweight (μg/ml), and all samples were diluted in DMSO. Dilutions weremade immediately before cell culture treatments and, in all cases, thefinal amount of DMSO did not exceed 1% in cell culture media.

Human endothelial kidney cells (HEK293) transfected with an NFκBluciferase reporter were challenged with TNFα for three hours, thensamples were applied to the challenged cells. The results are shown inFIGS. 1-3.

Cytotoxicity assays using the supernatants from the treated cells wereconducted using an LDH Cytotoxicity Detection Kit (Roche) according tothe manufacturer's instructions. The results are shown in FIGS. 4-6.

As shown in FIG. 1, TNFα induces an increase in NFκB-mediatedtranscription of luciferase; administration of anatabine can reduce thistranscription to control levels without cellular toxicity (FIG. 4).Crude extracts of smokeless tobacco, while not toxic to cells (FIG. 5),do not reduce TNFα-induced NFκB-mediated transcription (FIG. 2).Although not suitable for administration as pharmaceuticals, bothnicotine and an alkaloid extract of smokeless tobacco reduceTNFα-induced NFκB-mediated transcription (FIG. 3); at higher doses, thealkaloid extract demonstrates pronounced cytotoxicity (FIG. 6).

EXAMPLE 2 Materials and Methods

Animals. Male and female Sprague-Dawley rats (˜200-250 grams) wereobtained from Charles River Laboratories Inc., Wilmington, Mass. andused in compliance with the Animal Welfare Act, the Guide for the Careand Use of Laboratory Animals, and the Office of Laboratory AnimalWelfare. Upon receipt at the vivarium, rats were examined by trainedpersonnel to ensure acceptable health status. Rats were acclimated forat least 5 days prior to use.

Rats were housed 3 per cage. Cage size met or exceeded the requirementsset forth by the Institute for Animal Laboratory Research Guide for theCare and Use of Laboratory Animals. The rats were kept in a roommaintained at 64-84° F. (22-24° C.) with humidity set at 40-70%. Theroom was illuminated with fluorescent lights timed to give a 12hour-light, 12 hour-dark cycle. Standard rodent diet (PharmaServ labdiet 5001) and water were available for all rats. The feed was analyzedby the supplier, detailing nutritional information and levels ofspecified contaminants.

Test compounds. The following compounds were tested in the examplesbelow:

-   -   (−) Nicotine hydrogen tartrate (Sigma Aldrich: N5260        Lot#098K0676) 35.1% (w/w) nicotine;    -   (R,S) Anatabine tartrate (2:3) (Toronto Research Chemicals,        A637510, Lot#9-BHW-79-2) 41.6% (w/w) Anatabine;    -   (+/−)-nicotine-3′-d3 (Toronto Research Chemicals: N412423,        Lot#9-BCC-114-2);    -   (R,S)-Anatabine-2,4,5,6-d4 (Toronto Research Chemicals: A637505,        Lot#6-SG-82-1); and    -   anatabine polacrilex (Emerson Resource Inc. lot #JK02-145);        purity was 5.18% as per Certificate of Analysis

Certificates of analyses for anatabine and nicotine indicated 98% and100% purity, respectively. Anatabine was stored at 4° C. in a desiccatedenvironment (silica), protected from light. Nicotine was stored at roomtemperature. Vehicle was sterile phosphate buffered saline (PBS)(Amresco lot#2819B188).

Supplies. The following were obtained from Becton Dickinson, FranklinLakes, N.J.: MICROTAINER® Brand Tubes (K₂) EDTA (lot#9050883); serumseparator blood collection tubes (lot#9104015); and sodium citrate bloodcollection tubes (lot#8310564). Ten percent neutral-buffered formalinwas from Sigma Aldrich, St. Louis, Mo. (batch#019K4386).

EXAMPLE 3 Toxicokinetic Evaluation of Single Doses of Anatabine andNicotine in Sprague-Dawley Rats

This example reports evaluation of the toxicokinetics of anatabine andnicotine following a single intravenous injection in Sprague-Dawleyrats.

Summary

Anatabine was administered as a single intravenous (i.v.) injection atdoses of 0.10, 0.75, or 1.0 mg/kg. Nicotine was administered as a singleintravenous injection at a dose of 0.4 mg/kg. Six rats (3 males and 3females) were dosed per dose group. Blood was collected for plasma at15, 30, 60, 90, 120, 240, 360, 480, and 1440 minutes post i.v.administration. At the 1440 minute time point, animals were euthanizedand perfused, and brains were removed and then homogenized. Plasma andbrain homogenates were stored at −80° C. until analysis.

An additional 48 rats (24 males and 24 females) received a singleintravenous dose via the tail vein at the same doses as mentioned above.At 30 and 360 minutes post administration, 6 rats (3 males and 3females) per dose group, per time point were euthanized, bled viacardiac puncture, and perfused, and brains were collected. The brainswere homogenized. Blood was spun, and plasma was collected. Plasma andbrain homogenate were stored at −80° C.

Both anatabine and nicotine can be measured in rat plasma and brainfollowing a single bolus i.v. dose. The concentration of anatabine inplasma is dose-related. Both compounds are also rapidly cleared fromplasma; however, the elimination half-life of anatabine is approximately2- to 2.5-fold greater than that of nicotine (t_(1/2), 1.64 to 1.68 hrfor anatabine compared to 0.67 hr for nicotine). The apparent volume ofdistribution (V_(D)) for anatabine is also significantly greater thanthat of nicotine.

At all doses of anatabine the elimination half-life (t_(1/2)), meanresidence time (MRT), and exposures (AUC_(0→∞)) tended to be higher forfemale rats compared to male rats; however, only at the highest dose ofanatabine (1.0 mg/kg) was this difference statistically significant. Atthis dose level, the elimination half-life (t_(1/2)) of anatabine infemales was 1.84 hr compared to 1.44 hr for males; mean residence time(MRT) was 2.80 hr for females compared to 2.18 hr for males; andexposure (AUC_(0∝∞)) was 788.9 ng·hr/mL for females compared to 631.3ng·hr/mL for males.

Anatabine and nicotine rapidly appear in brain tissue following i.v.administration, and the concentration of anatabine is dose-dependent. Ateach dose level the mean concentration of anatabine appeared to behigher in the brains of female animals compared to males; however, thedifferences were not statistically significant.

Anatabine tartrate (2:3) or nicotine bitartrate was dissolved to theappropriate concentrations in sterile PBS for the i.v. formulations(Table 2). The dosing solutions for each test compound were prepared onthe basis of the relative content of the anatabine or nicotine base sothat the final concentrations are reflective of the actual baseconcentration. Four aliquots of each dose level formulation werecollected and stored at −80° C. The test compound, corresponding doselevel, number of animals, and sample collection times for Phase I of thestudy are shown in Table 3. The test compound, corresponding dose level,number of animals, and sample collection times for Phase II of the studyare shown in Table 4. The physical signs of each animal were monitoredfollowing administration of the test compound.

The animals were weighed prior to dosing and received a single i.v. doseof either test compound at a volume of 5 mL/kg. Blood was collected viathe venus plexus (retro-orbital) into tubes containing (K₂) EDTA. Nomore than 0.5 mL was collected per time point. For the 1440-minute timepoint of Phase I or the 30- and 360-minute time points of Phase II, theanimals were euthanized, bled via cardiac puncture, and perfused. Thebrain, was removed, weighed, homogenized in sterile 0.9% saline at avolume equal to its weight, and stored at −80° C.

Plasma was separated according to the instructions for MICROTAINER®brand collection tubes (3 minutes, 2000×g). Plasma was decanted intomicrofuge tubes and stored at −80° C. Remaining test compound was storedat −80° C.

Analytical Methods

The signal was optimized for each compound by electrospray ionization(ESI) positive or negative ionization mode. A single ion mode (SIM) scanwas used to optimize the Fragmentor for the precursor ion and a production analysis was used to identify the best fragment for analysis and tooptimize the collision energy. The fragment which gave the mostsensitive and specific signal was chosen.

Sample preparation. Plasma and brain samples were treated with threevolumes of methanol containing internal standard at 1 μM (either(+/−)-nicotine-3′-d₃ for nicotine or (R,S)-Anatabine-2,4,5,6-d₄ foranatabine), incubated 10 min at 4° C., and centrifuged. The amount ofthe test agent in the supernatant was determined by liquidchromatography tandem mass spectrometry (LC/MS/MS).

Analysis. Samples were analyzed by LC/MS/MS using an Agilent 6410 massspectrometer coupled with an Agilent 1200 high pressure liquidchromatography (HPLC) and a CTC PAL chilled autosampler, all controlledby MassHunter software (Agilent). After separation on a hydrophilicinteraction liquid chromatography (HILIC) HPLC column (Sepax) using anacetonitrile-ammonium acetate/acetic acid gradient system, peaks wereanalyzed by mass spectrometry (MS) using ESI ionization in multiplereaction monitoring (MRM) mode. MassHunter software was used tocalculate the concentration of the test compounds in samples from thepeak area using the appropriate calibration curves.

Recovery. Recovery standards were prepared by spiking blank matrix(plasma or brain homogenate) prior to deproteination or after with 23,62, or 1667 ng/mL of test compound. Deproteination was done by adding 3columns of methanol containing internal standard with centrifugation topellet the precipitated protein. Recovery was calculated by dividing thearea ratio (peak area of compound over internal standard of theprecipitated sample over the recovery standard multiplied by 100. Forexample: area ratio of spiked plasma/area ratio of spiked deproteinatedplasma×100.

Calibration samples. Calibration curves were determined for both ratplasma and brain homogenate. Calibration samples were prepared bydiluting a 50× stock solution of the test compound in PBS with blankmatrix to the appropriate concentration and these samples were preparedas described above in the sample preparation. Stock solutions wereprepared by serial dilution as shown in Table 5.

Results

Physical Signs. All males and two females that received nicotine at 0.4mg/kg experienced tremors immediately post dose and recovered within 2to 4 minutes. One male (7C) and two females (8A and 8C) in this groupalso experienced labored breathing which lasted 2 to 4 minutes postdose. The same male (7C) was lethargic and recovered approximately 8minutes post dose. All other animals in each dose group appeared normalfollowing the administration of the test compounds.

Method Development. Table 6 shows the results of the LC/MS/MS methoddevelopment for the determination of the appropriate ionizationconditions and the mass to charge ratios (m/z) of the parent and productions for anatabine and nicotine, and their deuterated analogues. Theindicated product m/z ratios were used for the analysis of the relevanttest samples.

The product ion spectra and sample chromatograms for each compound inTable 6 are shown in FIGS. 12-19. The limits of detection (LOD) ofanatabine and nicotine and their lower (LLQ) and upper (ULQ) limits ofquantitation were derived from the appropriate calibration curves foreach test compound and are shown in Table 7.

Table 8 provides data on the percent recovery of each test compound fromeither rat plasma or brain as a function of the given concentration.Except for the anatabine sample at the LOD and the nicotine samples inrat brain, recovery was generally greater than 90 percent.

Analysis of Dosing Solutions

Table 9 summarizes the analyses of the dosing solutions used in thisstudy. The percent differences between the actual and expectedconcentrations are shown. Except for the lowest dose of anatabine, whichwas 70% of the expected concentration, the actual concentrations of testcompounds were within 20% of the expected levels.

Plasma Pharmacokinetic Results & Analysis

Table 14 lists the plasma concentrations of anatabine and nicotine forall animals at each time point. Table 15 summarizes this data in termsof the mean plasma concentrations of the test compound at each timepoint for males, females and both genders combined. This data ispresented graphically in FIG. 7 and FIG. 8 (semi-log plot). The 24-hrdata points from all treatment groups were below the limits ofquantitation. Between approximately 6 and 8 hours the plasmaconcentrations of nicotine and anatabine (0.1 mg/kg) were below thelimits of quantitation.

Table 10 and Table 11 provide comparisons for several pharmacokineticparameters between the different treatment groups and between male andfemale animals. Both nicotine and anatabine can be measured in ratplasma following a single i.v. bolus, and their concentrations appear tobe dose-related. The elimination half-life (t_(1/2)) for each of theanatabine treatment groups was significantly greater than that for thenicotine treatment group (2.1× to 2.5× greater; 0.67 hr for nicotinecompared to 1.44 to 1.68 hr for anatabine). The elimination half-liveswere similar among the anatabine treatment groups. The longer half-lifefor anatabine is reflected in the longer mean residence times (MRT),which are about 2-fold longer for anatabine compared to nicotine.Finally, the apparent volume of distribution (V_(D)) was lower for thenicotine group compared to the anatabine treatment groups. Amongst theanatabine treatment groups, V_(D) was significantly greater for the 0.1mg/kg dose group compared to either of the two higher doses; however, itis not known whether this is a real difference or whether it is due tovariability and the fewer number of measurable data points at the lowdose.

Table 11 shows a comparison of these same parameters between male andfemale rats within each treatment group. There were no statisticallysignificant differences between males and females except in the highestanatabine treatment group (1.0 mg/kg) where the females exhibited alonger elimination half-life and therefore, longer mean residence timethan the males (t_(1/2), 1.84±0.16 hr and MRT, 2.80±0.24 hr, femalescompared to t_(1/2), 1.44±0.08 and MRT, 2.18±0.12 hr, males). Thisdifference is apparent for all treatment groups, although it onlyachieved statistical significance in the highest anatabine group. Thefemales in this treatment group also displayed a much greater overallexposure (AUC_(0→∞)) to anatabine than the male animals. This differenceis depicted in FIG. 9, which shows the dose-exposure relationship foranatabine and nicotine. Overall, there appears to be a linear responsebetween dose and exposure for anatabine; it is not possible to determineif the female animals display a non-linear response at high doses ofanatabine.

FIG. 11 shows the dose-concentration response for the 0.5-hour timepoint for males and females at each dose level. It appears that thebrain levels of anatabine begin to level off between 0.75 mg/kg and 1.0mg/kg.

Table 14 lists the concentrations of anatabine and nicotine in the brainextracts for all animals at each time point. Table 15 summarizes thisdata in terms of the mean concentrations of the test compound per gramof brain tissue at each time point for males, females and both genderscombined. This data is presented graphically in FIG. 10 and in tabularform in Table 12. After the 6-hour time point most concentrations werebelow the limits of quantitation; however, the test compoundconcentration was quantifiable in several samples at 24-hours.

FIG. 11 shows the dose-concentration response for the 0.5-hour timepoint for males and females at each dose level. It appears that thebrain levels of anatabine begin to level off between 0.75 mg/kg and 1.0mg/kg.

Discussion

All males and two females that received nicotine at 0.4 mg/kgexperienced tremors immediately post dose; however they recovered within2 to 4 minutes. One male (7C) and two females (8A and 8C) in this groupalso experienced labored breathing which lasted 2 to 4 minutes postdose. The same male (7C) was lethargic and recovered approximately 8minutes post dose. All animals in each of the anatabine dose groupsappeared normal immediately following administration of the testcompounds and no obvious adverse signs were observed.

Both nicotine and anatabine can be measured in rat plasma following asingle, bolus, i.v. dose and their concentrations appear to bedose-related. The elimination half-life of anatabine is approximately 2-to 2.5-fold greater than that of nicotine, and this is also reflected ina longer mean residence time, which is approximately twice as long asthat for nicotine. The 24-hr data points from all treatment groups werebelow the limits of quantitation and it appears that at the dosesselected, the test compounds are cleared from rat plasma between 8 and24 hours post-administration.

The apparent volume of distribution (V_(D)) was also significantly lowerfor the nicotine group compared to the anatabine treatment groups.Amongst the anatabine treatment groups, V_(D) was significantly greaterfor the 0.1 mg/kg dose group compared to either of the two higher doses;however, it is not known whether this is a real difference or whether itis due to variability and the fewer number of measurable data points atthe low dose.

When comparisons between male and female animals were conducted forthese same parameters, within each treatment group, there were nostatistically significant differences observed except for the highestanatabine treatment group (1.0 mg/kg) where the females exhibited alonger elimination half-life and therefore, longer mean residence timethan the males (t_(1/2), 1.84±0.16 hr and MRT, 2.80±0.24 hr, femalescompared to t_(1/2), 1.44±0.08 and MRT, 2.18±0.12 hr, males). In fact,these differences between male and female animals were apparent for alltreatment groups, although statistical significance was achieved only atthe highest anatabine dose tested. The females in this treatment groupalso displayed a much greater overall exposure (AUC_(0→∞)) to anatabinethan the male animals. Overall, there is a linear response between doseand plasma concentrations or exposure to anatabine in both male andfemale rats; although the response appears to be somewhat greater infemale animals and is more pronounced at the higher dose levels. It isnot possible to determine from the data if the female animals display anon-linear response at higher doses of anatabine.

Both anatabine and nicotine rapidly appear in brain tissue followingi.v. administration. The concentrations of anatabine are dose-dependentbut appear to level off between 0.75 mg/kg and 1.0 mg/kg. Thisobservation is based on the levels measured only at the 0.5-hour timepoint and a greater number of time points are required for a morethorough evaluation. There were no statistically significant differencesin the concentrations of either test compound in brain between male andfemale animals; however at each dose level the mean concentrations inthe brains of females tended to be somewhat higher.

EXAMPLE 4 Toxicokinetic Evaluation of Single Doses of Anatabine andNicotine with a 14-Day Observation Period

This example reports the evaluation of the toxicity of anatabine ornicotine for a period of fourteen days following a single intravenousinjection in Sprague-Dawley rats. The toxicity of anatabine and nicotinewas evaluated after a single intravenous (i.v.) injection in the rat.Anatabine was administered as a single intravenous injection at doses of0.10, 0.75, or 1.5 mg/kg. Nicotine was administered as a singleintravenous injection at a dose of 1.50 mg/kg. One control group ofanimals received a single i.v. dose of the vehicle at 5 mL/kg. Ten rats(5 males and 5 females) were dosed per group. Due to animal mortality inthe nicotine-dosed group, the surviving animals were taken off study anda separate nicotine tolerability study was conducted. One femalereceived a single i.v. dose of 1.25 mg/kg, and 3 females received asingle i.v. dose of 1.0 mg/kg. Following the tolerability study, a groupof 5 males and 5 females received a single i.v. dose of nicotine at 0.75mg/kg.

All rats dosed with vehicle or anatabine, and the animals dosed with0.75 mg/kg of nicotine were observed daily for 14 days. Body weight andfood consumption was measured daily for 14 days. On day 15, urine wascollected on all surviving animals. The animals were euthanized and bledvia cardiac puncture, and blood was collected for analysis. Tissues werecollected, weighed, evaluated for gross abnormalities, and stored in 10%neutral-buffered formalin.

All groups appeared normal immediately after dosing except for theanimals dosed with 1.5 mg/kg of anatabine and those dosed with 1.5 mg/kgof nicotine. Both males and females dosed with 1.5 mg/kg of anatabineexperienced tremors upon compound administration. The animals appearednormal by 15 minutes post dose. Upon completion of the 1.5 mg/kg dose ofnicotine, tremors and rigidity were observed in all dosed animals. Thetremors were more severe in the females. One male did not survive,whereas the other 4 appeared normal after 15 minutes. Three females weredosed and two died within 5 minutes of dosing; the remaining 2 femaleswere not dosed due to the morbidity in the group. The surviving animalsfrom this group were removed from study. These results suggest that bothanatabine and nicotine affect both the peripheral and central nervoussystems.

During the tolerability study, all rats (1 female dosed with 1.25 mg/kgof nicotine and 3 females dosed with 1.0 mg/kg of nicotine) experiencedsevere tremors upon completion of dosing, but all returned to normal by20 minutes post dose. These animals were not included in the 14-dayobservation period.

Both males and females dosed with nicotine at 0.75 mg/kg experiencedtremors upon compound administration but returned to normal within 15-20minutes post dose. One male and two females died post dose. Survivinganimals in all groups appeared normal throughout the 14-day observationperiod. The body weights for both male and female rats in the nicotinegroup were lower than those in the control and anatabine treatmentgroups; however, these were still within the study-specified range.Consequently body weight gain for this treatment group was also somewhatlower than the vehicle controls. Food consumption was similar among thegroups over the 14-day period; however, consumption by males treatedwith 0.1 mg/kg or 1.5 mg/kg anatabine appeared to be somewhat higherthan animals in the control group. This is not considered to be atreatment-related effect.

Hematology and blood chemistries for male and female animals wereanalyzed and evaluated for differences between the individual treatmentgroups and the relevant vehicle controls. All treatment groups showed nosignificant differences relative to the controls and/or the values werewell within the normal ranges expected for this species. Similarly, nonotable differences in any of the urinalysis parameters were observedbetween animals treated with either anatabine or nicotine, relative tothe controls.

Anatabine or nicotine was dissolved to the appropriate concentrations insterile PBS for the i.v. formulations (see Table 16). The dosingsolutions for each test compound were prepared on the basis of therelative content of the anatabine or nicotine base so that the finalconcentrations reflect the actual base concentrations. Four aliquots ofeach dose formulation were collected and stored at −80° C. The testcompound, corresponding dose level, number of animals, and frequency ofobservations are shown in Table 17.

The animals were weighed prior to dosing and received a single i.v. dosevia the lateral tail vein of either test compound or vehicle at a volumeof 5 mL/kg. Due to animal mortality in the nicotine-dosed group (1.5mg/kg), the surviving animals were taken off study and a separatenicotine tolerability study was conducted.

Nicotine Tolerability Study

One female rat was dosed intravenously with 1.25 mg/kg of nicotine, andthree females were received 1.0 mg/kg intravenously. Following thetolerability study, an additional group was added to the study. Fivemales and five females received a single intravenous dose of nicotine at0.75 mg/kg. All animals were observed daily. Body weight and foodconsumption was measured daily, with any abnormal observations noted.Average daily body weights and food consumption was tabulated withstandard deviation calculated.

On day 15, urine was collected on all surviving animals for urinalysis.The animals were euthanized and bled via cardiac puncture. Blood wascollected for hematology, clinical chemistry, and coagulation analysis.Tissues were collected, weighed, and stored in 10% neutral-bufferedformalin for possible future analysis. The tests and tissues collectedare summarized in Table 18.

Results

Dosing Solution Analysis

Table 19 summarizes the dosing solutions used during the conduct of thisstudy. The percent differences between the actual and expectedconcentrations of the test compounds are shown. The actualconcentrations were within 20 percent of the expected levels.

General Observations

All groups appeared normal immediately after dosing except for theanimals dosed with 1.5 mg/kg of anatabine and those dosed with 1.5 mg/kgof nicotine. Both males and females dosed with 1.5 mg/kg of anatabineexperienced tremors upon compound administration. The animals appearednormal by 15 minutes post dose. Following administration of the 1.5mg/kg dose of nicotine, tremors and rigidity were observed in allanimals. The tremors were more severe in the females. One male did notsurvive, whereas the other 4 appeared normal after 15 minutes. Threefemales in this group were dosed and two died within 5 minutes ofdosing; the remaining 2 females were not treated due to the observedmorbidity in the group. The surviving animals from this group wereremoved from the study.

During the tolerability study, all rats (1 female dosed with 1.25 mg/kgof nicotine and 3 females dosed with 1.0 mg/kg of nicotine) experiencedsevere tremors upon completion of dosing, but all returned to normal by20 minutes post dose. These animals were not included in the 14-dayobservation period.

Both males and females dosed with nicotine at 0.75 mg/kg experiencedtremors upon compound administration, but returned to normal within15-20 minutes post dose. One male and two females died post dose.

Surviving animals in all groups appeared normal throughout the 14-dayobservation period.

Body Weights, Growth Rates and Food Consumption

The daily measured body weights for each animal are tabulated in Tables28A-F and the average daily food consumption is summarized in Tables29A, B. These data are summarized in Table 20 for the average weightgain over the 14-day observation period and the average daily foodconsumption, by treatment group and gender. FIG. 20 shows the mean bodyweights of animals in each treatment group on the day of dosing (Day 0)and for each day, thereafter.

The average weight gains for animals in each treatment group over the14-day observation period were similar to those in the vehicle controlgroup, except for the nicotine-dosed group of male animals thatexhibited weight gains that were significantly lower than the controls.The mean increase in the weight of females of the nicotine-dosed groupwas also lower than that of the vehicle control, though notstatistically significant at the 5 percent level. It should be notedthat the mean weights of the male and female animals in thenicotine-treated group at Day 0 were lower than their correspondinggenders in the vehicle control. The difference for males wasstatistically significant (Vehicle: 234.6±9.9 g versus Nicotine:216.0±6.2 g; p=0.014), although that for females was not (Vehicle:209.8±7.3 g versus Nicotine: 195.3±10.4 g; p=0.058).

The average daily food consumption per animal was statistically higherin the males of the 0.1 mg/kg and 1.5 mg/kg anatabine treatment groups.This difference is not considered to be clinically significant orrelated to any treatment effects.

Overall, although some differences in the changes in weight and foodconsumption were statistically significant, they are not considered tobe treatment-related.

Necropsy Observations and Organ Weights

Upon necropsy and organ collection no noticeable differences orabnormalities were observed between the vehicle-dosed animals and thetest compound-dosed animals. Individual organ weights can be found inTable 36. Several statistically significant differences in organ weightswere noted (see Table 21 and Table 22); however, they do not appear tobe dose-related and likely due to the small sample sizes and variabilityin the organ collection. In general, several organ weights tended to belower in the nicotine-treated group, although this observation is likelyrelated to the lower animal weights in this group relative to thecontrols.

Hematology and Coagulation Parameters

Plasma samples collected for hematology were analyzed, and individualvalues for the various parameters for each animal are listed in Table 31(normal ranges, Table 30) and these are summarized in terms ofdescriptive statistics in Table 23A, Table 23B, and Table 24. Also shownare statistical comparisons between the vehicle controls and the varioustreatment groups, subdivided by gender.

In general, there were few significant differences between the treatmentgroups and the vehicle control group for either gender. Female rats in0.1 mg/kg anatabine group showed a small but statistically significantdecrease in mean corpuscular hemoglobin concentration (MCHC) relative tothe control; however, the values are still within the normal range forthis species. Similarly, females in the 1.5 mg/kg anatabine and 0.75mg/kg nicotine treatment groups showed small, but statisticallysignificant decreases in mean corpuscular volume (MCV) and meancorpuscular hemoglobin (MCH), although these values were still withinthe normal range for this species as well.

Males and females in the 0.75 mg/kg and 1.5 mg/kg anatabine groupsshowed a statistically significant decrease in reticulocyte countcompared to the control animals; however, these values are also wellwithin the normal range for this parameter.

There were no notable differences in red blood cells, white blood cells,platelet counts, lymphocyte, monocyte, eosinophil and basophil counts,or neutrophil segmentation.

Individual values for the coagulation parameters activated partialthromboplastin (aPTT) and prothrombin times (PT) for each animal arelisted in Table 34 (normal ranges, Table 30). These are summarized interms of descriptive statistics in Table 25. Also shown are statisticalcomparisons between the vehicle controls and the various treatmentgroups, subdivided by gender. There were no significant differences inaPTT or PT between the vehicle control and each of the anatabinetreatment groups; although the aPTT values for all these groups wereoutside the normal range. In both male and female animals of thenicotine group, however, aPTT was significantly lower relative to thevehicle control group, indicative of faster clotting times due to theintrinsic, contact activation pathway. The origin of this difference isnot known, although the values are within the normal range for thisspecies.

Clinical Chemistry

Plasma samples collected for blood chemistries were analyzed, andindividual values for the various parameters for each animal are listedin Table 33 (normal ranges, Table 32), and these are summarized in termsof descriptive statistics in Tables 26A, 26B, 27A, and 27B. Also shownare statistical comparisons between the vehicle controls and the varioustreatment groups, subdivided by gender.

Values for all clinical chemistry parameters were within the respectivenormal ranges. There were several parameters where statisticallysignificant differences were noted between treatment groups andcontrols. Specifically, males treated with anatabine at 0.75 mg/kg and1.5 mg/kg showed slight increases in albumin levels, as did femalestreated with 0.1 mg/kg and 0.75 mg/kg anatabine, but not at 1.5 mg/kg.Total protein was slightly increased in males in all anatabine treatmentgroups and the nicotine group relative to vehicles controls. In females,total protein was somewhat higher only in the 0.1 mg/kg anatabine andnicotine groups. Finally, as with total protein, globulins weremarginally higher at all anatabine dose levels and the nicotine dosegroup in males. Globulins were also slightly higher in females in the0.1 mg/kg anatabine and nicotine groups. The higher globulin levels, butnot albumin, in the nicotine group is reflected in slightly lower A/Gratios, for both genders. Nevertheless, all the reported values foralbumin, globulins and total protein were within the normal range forthis species. There were small, but statistically significantdifferences noted for calcium levels in males in the nicotine-treatedgroup and for sodium levels in males at 0.75 mg/kg and 1.5 mg/kganatabine and females in the 1.5 mg/kg anatabine treatment groups. Thevalues are well within normal ranges and therefore, not clinicallysignificant.

Urinalysis

Individual values of the urinalysis parameters for each animal arelisted in Table 35. There were no notable differences between the activetreatment groups and controls and the observations are all consistentwith those expected for this species.

Discussion

The toxicity of anatabine and nicotine was evaluated after a singleintravenous (i.v.) injection in the rat. Anatabine was administered atdoses of 0.10, 0.75, or 1.5 mg/kg. Nicotine was administered at a doseof 1.50 mg/kg, initially; however, due to mortality and significantadverse effects observed at this dose and at lower doses of 1.0 mg/kgand 1.25 mg/kg, a separate group was included in the study and dosedwith nicotine at 0.75 mg/kg. One group of animals received a single i.v.dose of the vehicle at 5 mL/kg. Ten rats (5 males and 5 females) weredosed per group.

All rats dosed with vehicle or anatabine, and the animals dosed with0.75 mg/kg of nicotine were observed daily for 14 days. Body weight andfood consumption was measured daily for 14 days. On day 15, urine wascollected on all surviving animals. The animals were euthanized, bledvia cardiac puncture, and blood was collected for analysis. Tissues werecollected, weighed, any gross abnormalities were noted, and stored in10% neutral-buffered formalin for possible future analysis.

All animals, at all dose levels of anatabine, survived the study;however, those in the 1.5 mg/kg anatabine group experienced tremors andshaking immediately after test compound administration, which lasted forapproximately 15 minutes post-treatment. In the nicotine treatment group(0.75 mg/kg), one male animal and 2 females died following test compoundadministration, and all animals experienced tremors and shaking for upto 20 minutes post-administration. These results suggest that bothanatabine and nicotine affect both the peripheral and central nervoussystems.

The growth rates and food consumption in all anatabine treatment groupswere similar to their appropriate male or female vehicle controls. Malerats in the nicotine treatment group had a slightly lower growth rate;however, this is unlikely to be related to the test compound. This groupof animals began the study at a lower average weight than males in thecontrol or anatabine treatment groups. The food consumption in males, inthe 0.1 mg/kg and 1.5 mg/kg anatabine groups was somewhat higher thancontrols and although the result was statistically significant it is notlikely to be related to an effect of the test compound.

At necropsy, no noticeable differences or gross abnormalities wereobserved in any of the organs collected between the vehicle-treated andthe test compound-treated animals. Several statistically significantdifferences in organ weights were noted; however, they do not appear tobe dose-related and are likely due to the small sample sizes and theinherent variability associated with organ collection. The weights ofheart, liver and kidneys in males, and thymus and heart in females ofthe nicotine-treated group were significantly lower than those of thecorresponding vehicle controls; however, this observation is likelyrelated to the lower overall animal weights in this group relative tothe controls.

The hematology parameters for all treatment groups and genders werewithin the normal ranges expected for this species or displayed nosignificant differences when compared to the vehicle controls. Activatedpartial thromboplastin and prothrombin times were similar for allanatabine treatment groups relative to the controls; however, they werehigher than the expected normal range. Both males and females in thenicotine group displayed significantly shorter clotting times via theintrinsic or contact activation pathway (aPTT) compared to the relevantcontrol animals; however, the values were within the normal ranges forthis species. Clotting times via the extrinsic or tissue factor pathwayas determined by prothrombin times (PT) were normal.

Values for all clinical chemistry parameters were within the respectivenormal ranges or showed no differences relative to the vehicle controlgroup.

Evaluation of the individual urinalysis parameters for each animalshowed no notable differences between the active treatment groups andcontrols.

EXAMPLE 5 Toxicokinetic Evaluation in Sprague-Dawley Rats of OralMulti-Dose Administration of Anatabine

This example reports the results of an evaluation of thepharmacokinetics of anatabine following multiple oral doses inSprague-Dawley rats.

Summary

The plasma pharmacokinetic profile of orally administered anatabine wasinvestigated in the rat. This study consisted of two groups of 8 animalseach, 4 males and 4 females. One group received a total of 0.6 mganatabine per kilogram body weight (BW) and the second group received6.0 mg anatabine per kilogram BW in three, divided, oral, doses of 0.2mg/kg BW (0.6 mg total) or 2.0 mg/kg BW (6.0 mg total). The testcompound was administered as anatabine polacrilex and each dose wasadministered at 0, 4, and 8 hours and was administered in a volume of 5mL/kg BW. Blood was collected for plasma at 30, 60, 240, 270, 300, 480,540, 600, 720 and 1440 minutes post initial dose.

All animals in both treatment groups appeared normal immediatelyfollowing each administration of the test compound and no adverse signswere observed for the duration of the observation and plasma samplingperiod.

The mean time to maximal plasma concentration following the first twooral doses ranged from 0.50 to 0.88±0.25 hr. There were no significantdifferences between gender or dose group. After the third dose of testcompound, the mean time to maximal plasma concentration ranged from 1.00to 2.00±1.41 hr. Within each dose group there were no significantdifferences in C_(p, max) between males and females and nor was thereany significant change in this parameter over time. In females of thehigh dose group C_(p, max) appeared to increase from 259.8±35.4 ng/mL to374.8±122.9 ng/mL; however, the trend was not statistically significant.

There were two, observable, minima following the first two oral doses ofanatabine polacrilex. In general, the minima were not significantlydifferent from one another over time, except for females of the highdose group, which increased from 51.5±26.0 ng/mL to 180±31 ng/mL.

The total exposure, elimination half-lives, mean transit times and meanabsorption times did not differ significantly between male and femalerats within the two treatment groups. When these data are combined andgrouped according to dose level the total exposure is significantlygreater at the high dose as would be expected; however, the terminalelimination half-life is also significantly higher in the 6.0 mg/kg BWgroup compared to the 0.6 mg/kg BW dose group.

The overall elimination half-life of anatabine following the first oraldose was 1.93±0.73 hr, the mean transit time was 3.01±1.25 hr and themean absorption time was 0.56±1.25 hr. The mean absorption time of 0.56compares favorably with the calculated T_(max) values following thefirst two doses and indicates that the absorption of anatabine occurswithin the first 30 to 60 minutes after oral administration.

Anatabine was stored at 4° C., protected from light. The vehicle wassterile phosphate buffered saline (PBS) (Amresco). The test compound wasformulated in sterile phosphate buffered saline (PBS) based on thecontent of anatabine base in the anatabine polacrilex. Two formulationswere prepared; one for each of the two treatment groups. The testcompound was formulated for each treatment group just prior to the firstdose administration and constantly stirred until dosing was completed(Table 37). Four aliquots of each dose level formulation were collectedand stored at −80° C. The test compound, corresponding dose level, andnumber of animals are shown in Table 38. The sample collection times areshown in Table 39.

The physical signs of each animal were monitored followingadministration of the test compound.

The animals were weighed prior to dosing and received three doses p.o.of test compound at a volume of 5 mL/kg. Blood was collected via thevenus plexus (retro-orbital) into tubes containing (K₂) EDTA. No morethan 0.5 mL was collected per time point. For the 1440-minute time pointthe animals were euthanized, and bled via cardiac puncture.

Plasma was separated as per package instructions for MICROTAINER® brandcollection tubes (3 minutes, 2000×g). Plasma was decanted into microfugetubes and stored at −80° C. Remaining test compound was placed at −80°C.

Sample preparation. Plasma samples were treated with three volumes ofmethanol containing internal standard at 1 μM(R,S)-Anatabine-2,4,5,6-d₄), incubated 10 min at 4° C., and centrifuged.The amount of the test agent in the supernatant was determined byLC/MS/MS.

Analysis. Samples were analyzed by LC/MS/MS using an Agilent 6410 massspectrometer coupled with an Agilent 1200 high pressure liquidchromatography (HPLC) and a CTC PAL chilled autosampler, all controlledby MassHunter software (Agilent). After separation on a Hydrophilicinteraction liquid chromatography (HILIC) HPLC column (Sepax) using anacetonitrile-ammonium acetate/acetic acid gradient system, peaks wereanalyzed by mass spectrometry (MS) using ESI ionization in multiplereaction monitoring (MRM) mode. MassHunter software was used tocalculate the concentration of the test compounds in samples from thepeak area using the appropriate calibration curves.

Calibration samples. Calibration curves were determined in rat plasma.Calibration samples were prepared by diluting a 50× stock solution ofthe test compound in PBS with blank matrix to the appropriateconcentration and these samples were prepared as described above in thesample preparation. Stock solutions were prepared by serial dilution asshown in Table 40.

Data Analysis. Descriptive statistics were calculated for allpharmacokinetic parameters. Elimination half-lives (t_(1/2)) werecalculated by linear regression of logarithmically transformed plasmaconcentration data for each period between doses and following the finaldose.

Total areas under the plasma concentration curves (AUC) and under thefirst moment curves (AUMC) were calculated using linear trapezoidalsummation across all concentration time points as well as for intervalsbetween each dose administration and following the final dose. For theinterval following the first oral dose of anatabine polacrilex, meantransit times (MTT) were calculated from the corresponding ratio of AUMCto AUC. Mean absorption times (MAT) were calculated according to thefollowing relation:

MAT=MTT−MRT,

where MRT represents the mean residence time. This was calculated fromthe mean residence times.

The statistical comparison of parameters between male and female animalswas made using a two-tailed, unpaired, t-test with a 95 percentconfidence interval. Repeated-measures analysis of variance (ANOVA) wasused for multiple comparisons of C_(p, max) involving successivedeterminations on the same group of animals.

Results

Physical Signs. No adverse events were observed.

Method Development. Table 41 shows the results of the LC/MS/MS methoddevelopment for the determination of the appropriate ionizationconditions and the mass to charge ratios (m/z) of the parent and productions for anatabine and its deuterated analogue as determined above. Theindicated product m/z ratios were used for the analysis of the relevanttest samples.

See Example 3 for the product ion spectra and sample chromatograms foreach compound in Table 41. The limits of detection (LOD), lower (LLQ),and upper (ULQ) limits of quantitation was derived from the calibrationcurve and are shown in Table 42.

Analysis of Dosing Solutions. Table 43 provides a summary of theanalyses of the dosing solutions used during the conduct of this study.The percent differences between the actual and expected concentrationsare shown. The lowest dose of anatabine, which was 63% of the expectedconcentration and the high dose was 84% of the expected level.

Plasma Pharmacokinetic Results & Analysis. FIG. 21A and FIG. 21B showthe mean plasma anatabine concentration-time curves for male and femalerats in each of the two dose groups: 0.6 mg/kg (FIG. 21A) and 6.0 mg/kgBW (FIG. 21B). FIG. 22A and FIG. 22B show the same data with the valuesfrom both males and females combined. In each instance, three plasmaconcentration maxima can be observed corresponding to the administrationof the three divided doses of anatabine polacrilex at 0, 4 and 8 hours.Similarly, two anatabine plasma concentration minima are found prior toadministration of the final dose.

The mean maxima and minima anatabine plasma concentrations (C_(p, max),C_(p, min)) for males and females in each dose group are recorded inTable 44 along with the mean time to maximal concentration followingeach of the three doses (T_(max)). Statistical comparisons between maleand female animals within each dose group revealed no significantdifferences in any of the parameters, except for the second plasmaconcentration minimum (C_(p, min(2))) in both treatment groups; 15.3±5.5ng/mL versus 7.5±1.7 ng/mL in the 0.6 mg/kg BW treatment group, and93±16 ng/mL versus 180±31 ng/mL in the 6.0 mg/kg BW treatment group.FIG. 23A and FIG. 23B show the data in Table 44 plotted as a function oftime.

The times to reach maximal concentration generally occurred within 0.5hr and 1.0 hr post administration in both treatment groups and for bothgenders, following doses one and two (see Table 45). After the thirddose, t_(max(3)) was generally between 1.0 and 2.0 hourspost-administration; however, it should be noted that the earliestsampling point was at 1 hr following this dose.

Table 45 shows a comparison of the plasma concentration maxima andminima over time for male and female rats in both treatment groups.There were no statistically significant changes in any of theseparameters except for the plasma concentration minima for female rats inthe high dose group; C_(p, min) increased from 51.5±26.0 ng/mL to180.0±30.7 ng/mL.

The mean exposures (AUC), elimination half-lives (t_(1/2)), mean transittimes (MTT) and mean absorption times (MAT) are reported in Table 46 formale and female animals in the two treatment groups. There are nosignificant differences between the genders in any parameter, at eitherdose level.

When the male and female data are combined, as shown in Table 47, thereis a significant difference in total exposure as would be expected as aconsequence of the two different dose levels (AUC_(0→∞); 285±77 ng·hr/mLversus 3496±559 ng·hr/mL). There is also a significant difference in theterminal elimination half-life between the two treatment groups(t_(1/2, terminal); 1.79±0.64 hr versus 4.53±1.77 hr), wheret_(1/2, terminal) refers to the elimination half-life following thefinal dose of anatabine polacrilex.

As there were no significant differences in the calculated eliminationhalf-life, mean transit times and mean absorption times betweentreatment groups following the first dose of the test compound(t_(1/2, 0→4), MTT_(0→4), and MAT_(0→4), respectively), the data at bothdose levels were combined for males and females (see Table 48). Therewere no significant differences in these parameters between genders.

Table 49 provides animal weights and dosing times. Table 50 providesmeasured concentrations of anatabine in rat plasma samples at each timepoint. Table 51 provides mean concentration and description statisticsof anatabine in plasma samples at each time point.

The data from both genders are also combined to give correspondingoverall values. The calculated mean elimination half-life (t_(1/2, 0→4))is 1.93±0.73 hr, the mean transit time (MTT_(0→4)) is 3.01±1.25 hr, andthe mean absorption time (MAT_(0→4)) is 0.56±1.25 hr.

Discussion

This study evaluated the pharmacokinetics of anatabine in male andfemale Sprague-Dawley rats following the repeat-dose administration ofanatabine polacrilex by oral gavage at two different dose levels.Anatabine was administered at 0.6 mg/kg BW in three, divided, doses of0.2 mg/kg BW, or at 6.0 mg/kg BW in three, divided, doses of 2.0 mg/kgBW. Each dose was separated by an interval of four hours. All animals inboth treatment groups appeared normal immediately following eachadministration of the test compound and no adverse signs were observedfor the duration of the observation and plasma sampling period.

Anatabine concentrations can be measured in rat plasma following singleand repeat oral dosing. The mean time to maximal plasma concentrationfollowing the first two oral doses ranged from 0.50 to 0.88±0.25 hr.There were no significant differences between gender or dose group.After the third dose of test compound, the mean time to maximal plasmaconcentration ranged from 1.00 to 2.00±1.41 hr; although in thisinstance the first time point measured was at one hour post-dose andtherefore, it is possible that actual maximum occurred prior to thistime. Within each dose group there were no significant differences inC_(p, max) between males and females, nor was there any significantchange in this parameter over time. In females of the high dose groupC_(p, max) appeared to increase from 259.8±35.4 ng/mL to 374.8±122.9ng/mL; however, the trend was not statistically significant.

There were also two, observable, minima following the first two oraldoses of anatabine polacrilex. In general, the minima were notsignificantly different from one another over time, except for femalesof the high dose group, which increased from 51.5±26.0 ng/mL to 180±31ng/mL. Overall, these results suggest that with a 4-hour dosinginterval, and after eight hours, near steady-state conditions appearhave been achieved in male animals, whereas in females this may not yetbe the case.

Within the two treatment groups, the total exposure, eliminationhalf-lives, mean transit times and mean absorption times did not differsignificantly between male and female rats. When these data are combinedand grouped according to dose level the total exposure is significantlygreater at the high dose as would be expected; however, the terminalelimination half-life is also significantly higher in the 6.0 mg/kg BWgroup compared to the 0.6 mg/kg BW dose group. The reason for thisdifference is not apparent since the mean transit times and meanabsorption times did not differ significantly.

The elimination half-life, mean transit time and mean absorption timefollowing the first oral dose of the test compound are the most reliableestimates of these parameters since the plasma concentration data arenot confounded by carry-over amounts from a previous dose. The overallelimination half-life of anatabine following the first oral dose was1.93±0.73 hr, the mean transit time was 3.01±1.25 hr and the meanabsorption time was 0.56±1.25 hr. The mean absorption time (also oftencalled mean arrival time) of 0.56 compares favorably with the calculatedT_(max) values following the first two doses and indicates that theabsorption of anatabine occurs within the first 30 to 60 minutes afteroral administration.

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TABLE 2 Dosing solutions Test Test compound compound Percentage concen-concen- content of tration tration Injection Test anatabine or Doselevel (total) (base) volume compound nicotine base (mg/kg) (mg/mL)(mg/mL) (mL/kg) Anatabine 41.6 0.10 0.048 0.020 5 Anatabine 41.6 0.750.36 0.15 5 Anatabine 41.6 1.0 0.48 0.20 5 Nicotine 35.1 0.4 0.23 0.0815

TABLE 3 Phase I Collection Dose level Number of times Test compoundRoute (mg/kg) animals (M/F) (minutes)^(a) Anatabine i.v. 0.10 3/3 15,30, 60, 90, 120, 240, 360, 480, 1440 Anatabine i.v. 0.75 3/3 15, 30, 60,90, 120, 240, 360, 480, 1440 Anatabine i.v. 1.0 3/3 15, 30, 60, 90, 120,240, 360, 480, 1440 Nicotine i.v. 0.4 3/3 15, 30, 60, 90, 120, 240, 360,480, 1440 ^(a)Plasma samples were collected at all time points,. Braintissue was collected at 1440 minutes.

TABLE 4 Phase II Number of animals Collection Dose level per time pointtimes Test compound Route (mg/kg) (M/F) (minutes)^(a) Anatabine i.v.0.10 3/3 30, 360 Anatabine i.v. 0.75 3/3 30, 360 Anatabine i.v. 1.0 3/330, 360 Nicotine i.v. 0.4 3/3 30, 360 ^(a)Plasma samples and braintissue were collected at all time points.

TABLE 5 Calibration Curve Concentrations nominal concentration stockconcentration (ng/mL) (μg/mL) 5000 250 1667 83.3 555.5 27.8 185.2 9.361.7 3.1 20.6 1.0 6.9 0.34 2.3 0.11 0.76 0.038 0.25 0.013

TABLE 6 LC/MS/MS ionization conditions and identity of parent andproduct ions Collision Precursor Product energy Compound MW Polarizationm/z m/z (V) Anatabine 160.2 Positive 161.1 115.1 28 Nicotine 162.3Positive 163.1 117.1 28 (+/−)-nicotine- 165.25 Positive 166.1 118 283′-d₃ (R,S)- 164.24 Positive 165.1 148.1 20 Antabine- 2,4,5,6-d₄

TABLE 7 Limits of Detection and Calibration Curves Lower Limit of UpperLimit of Quantitation Quantitation Limit of Detection (LLQ) (ULQ) Sample(LOD) (ng/mL) (ng/mL) (ng/mL) Anatabine in rat 0.76 2.3 5000 plasmaAnatabine in rat 0.76 2.3 5000 brain Nicotine in rat 0.76 2.3 5000plasma Nicotine in rat 0.76 2.3 5000 brain

TABLE 8 Recovery from Plasma % Recovery at Given Concentrations Sample2.3 ng/mL 62 ng/mL 1667 ng/mL Anatabine in rat plasma 74 96 ND^(a)Anatabine in rat brain ND 96 90 Nicotine in rat plasma ND 105 104Nicotine in rat brain ND 78 84 ^(a)ND—not determined; two points percondition were evaluated for measuring recovery.

TABLE 9 Dosing Solution Analysis Actual Concentration Expected Actualrelative to Dose Concentration Concentration Expected Compound (mg/kg)(mg/mL) (mg/mL) (%) Nicotine 0.4 0.081 0.096 118.5 Nicotine 0.4 0.0810.096 118.5 Anatabine 0.1 0.02 0.014 70 Anatabine 0.75 0.15 0.135 90Anatabine 1 0.2 0.177 88.5 Anatabine 0.1 0.02 0.015 75 Anatabine 0.750.15 0.133 88.7 Anatabine 1 0.2 0.162 81

TABLE 10 Statistical Comparison of the Pharmacokinetic ParametersNicotine (0.4 mg/kg) Anatabine (0.1 mg/kg) Anatabine (0.75 mg/kg)Anatabine (1.0 mg/kg) Parameter M + F p M + F p M + F p M + F AUC_(0→∞)156.5 ± 32.6  35.0 ± 11.6 504.4 ± 63.5  710.07 ± 88.4  (ng · hr/mL)t_(1/2) (hr) 0.67 ± 0.07 0.003^(a) 1.44 ± 0.48 0.25^(d) 1.68 ± 0.090.69^(f) 1.64 ± 0.25 <0.001^(b) 0.39^(e) <0.001^(c) MRT (hr) 1.22 ± 0.130.004^(a) 2.29 ± 0.07 0.35^(d) 2.58 ± 0.14 0.63^(f) 2.49 ± 0.38<0.001^(b) 0.55^(e) <0.001^(c) V_(D) (L/kg) 2.06 ± 0.13 <0.001^(a) 6.08± 0.45 <0.001^(d) 3.33 ± 0.13 0.15^(f) 3.08 ± 0.16 <0.001^(b) <0.001^(e)<0.001^(c) ^(a)Nicotine vs. Anatabine (0.1 mg/kg) ^(b)Nicotine vs.Anatabine (0.75 mg/kg) ^(c)Nicotine vs. Anatabine (1.0 mg/kg)^(d)Anatabine (0.1 mg/kg) vs. Anatabine (0.75 mg/kg) ^(e)Anatabine (0.1mg/kg) vs. Anatabine (1.0 mg/kg) ^(f)Anatabine (0.75 mg/kg) vs.Anatabine (1.0 mg/kg)

TABLE 11 Comparison of Pharmacokinetic Parameters (±Std Dev) betweenmale and female animals in each Treatment Group Anatabine Nicotine (0.4mg/kg) Anatabine (0.1 mg/kg) (0.75 mg/kg) Parameter male female p malefemale p male AUC_(0→∞) 140.5 ± 5.8  172.6 ± 43.1  0.27 32.0 ± 7.7  37.9± 15.9 0.59 464.4 ± 36.2  (ng · hr/mL) t_(1/2) (hr) 0.66 ± 0.11 0.68 ±0.02 0.81 1.25 ± 0.32 1.64 ± 0.59 0.37 1.64 ± 0.12 MRT (hr) 1.21 ± 0.201.22 ± 0.05 0.90 2.03 ± 0.41 2.55 ± 0.93 0.42 2.50 ± 0.19 V_(D) (L/kg)2.10 ± 0.20 1.91 ± 0.17 0.54 5.29 ± 0.49 6.52 ± 0.66 0.22 3.48 ± 0.18Anatabine (0.75 mg/kg) Anatabine (1.0 mg/kg) Parameter female p malefemale p AUC_(0→∞) 544.5 ± 62.7  0.13 631.3 ± 28.2  788.9 ± 9.3  <0.001(ng · hr/mL) t_(1/2) (hr) 1.73 ± 0.03 0.28 1.44 ± 0.08 1.84 ± 0.16 0.02MRT (hr) 2.65 ± 0.01 0.25 2.18 ± 0.12 2.80 ± 0.24 0.02 V_(D) (L/kg) 3.19± 0.15 0.38 3.01 ± 0.12 3.16 ± 0.15 0.29

TABLE 12 Mean (ng/g ± Std Dev) concentrations of nicotine and anatabinein rat brain extracts following a single, bolus, i.v. dose TreatmentGroup Nicotine Anatabine Anatabine Anatabine 0.4 mg/kg 0.1 mg/kg 0.75mg/kg 1.0 mg/kg Time (hr) Male Female Male Female Male Female MaleFemale 0.5 94.3 ± 20.6 120.0 ± 3.0 20.0 ± 1.4 29.7 ± 4.5 276.0 ± 37.0314.7 ± 67.9 323.0 ± 35.9  346.0 ± 56.7 6 6.0 ± 1.4 5.0 3.0  3.7 ± 1.521.3 ± 5.1 21.0 ± 6.2 5.0 ± 2.6  6.0 ± 2.8 24 6.3 ± 2.3 7.0 3.0 2.0 <LLQ<LLQ 2.5 ± 0.7 <LLQ

TABLE 13A Rat PK i.v. dose-Brain Collection Compound: Anatabine, NicotiDose: 5 mL/kg Route: i.v. PBS Dose 24 hr Cmpnd Rat B.W. (g) volume (mL)time time Brain wt (g) Volume (mL) 1 A 245 1.23 8:17 8:17 1.74 1.74 MALEB 247 1.23 8:19 8:19 1.88 1.88 Anatabine C 238 1.20 8:21 8:21 1.80 1.800.1 mg/kg 2 A 205 1.03 8:23 8:23 1.68 1.68 FEMALE B 211 1.05 8:25 8:251.83 1.83 Anatabine C 202 1.00 8:27 8:27 1.66 1.66 0.1 mg/kg 3 A 2551.28 8:29 8:29 1.90 1.90 MALE B 223 1.13 8:31 8:31 1.82 1.82 Anatabine C242 1.20 8:33 8:33 1.84 1.84 0.75 mg/kg 4 A 204 1.03 8:35 8:35 1.82 1.82FEMALE B 205 1.03 8:37 8:37 1.82 1.82 Anatabine C 210 1.05 8:39 8:391.71 1.71 0.75 mg/kg 5 A 242 1.20 8:41 8:41 1.83 1.83 MALE B 251 1.258:43 8:43 1.85 1.85 Anatabine C 246 1.23 8:45 8:45 1.90 1.90 1.0 mg/kg 6A 213 1.08 8:47 8:47 1.95 1.95 FEMALE B 218 1.10 8:49 8:49 1.75 1.75Anatabine C 219 1.10 8:51 8:51 1.91 1.91 1.0 mg/kg 7 A 242 1.20 8:548:54 2.03 2.03 MALE B 241 1.20 8:56 8:56 1.98 1.98 Nicotine C 252 1.258:58 8:58 1.86 1.86 0.4 mg/kg 8 A 219 1.10 9:00 9:00 1.82 1.82 FEMALE B215 1.08 9:02 9:02 1.87 1.87 Nicotine C 220 1.10 9:04 9:04 1.87 1.87 0.4mg/kg Control 1 N/A N/A N/A N/A 1.83 1.83 Male 2 N/A N/A N/A N/A 1.941.94 3 N/A N/A N/A N/A 1.82 1.82

TABLE 13B Animal Weights and Dosing Times Rat PK i.v. dose-BrainCollection Dose: 5 mL/kg Compound: Anatabine, Nicotine Route: i.v., PBSDose 0.5 hour Cmpnd Rat B.W.(g) volume (mL) time time Brain wt (g)Volume (mL) 1 D 264 1.30 12:38 13:08 1.58 1.58 MALE E 270 1.35 12:4113:11 1.54 1.54 Anatabine 0.1 mg/kg F 252 1.26 12:45 13:15 1.69 1.69 2 D220 1.10 12:46 13:16 1.78 1.78 FEMALE E 206 1.03 12:50 13:20 1.54 1.54Anatabine 0.1 mg/kg F 214 1.08 12:52 13:22 1.69 1.69 3 D 259 1.30 12:5613:26 1.70 1.70 MALE E 266 1.33 12:58 13:28 1.66 1.66 Anatabine 0.75mg/kg F 264 1.33 13:03 13:33 1.46 1.46 4 D 208 1.05 13:05 13:35 1.811.81 FEMALE E 219 1.10 13:09 13:39 1.84 1.84 Anatabine 0.75 mg/kg F 2231.13 13:12 13:42 1.69 1.69 5 D 276 1.38 13:16 13:46 2.00 2.00 MALE E 2521.25 13:19 13:49 1.84 1.84 Anatabine 1.0 mg/kg F 255 1.28 13:22 13:521.68 1.68 6 D 212 1.05 13:25 13:55 1.66 1.66 FEMALE E 225 1.13 13:2913:59 1.56 1.56 Anatabine 1.0 mg/kg F 236 1.18 13:32 14:02 1.79 1.79 7 D273 1.38 13:36 14:06 1.76 1.76 MALE E 256 1.28 13:39 14:09 1.72 1.72Nicotine 0.4 mg/kg F 263 1.33 13:44 14:14 1.77 1.77 8 D 212 1.05 13:4814:18 1.75 1.75 FEMALE E 213 1.05 13:52 14:22 1.81 1.81 Nicotine 0.4mg/kg F 231 1.15 13:59 14:29 1.90 1.90

TABLE 14 Measured Concentrations of Anatabine and Nicotine in Rat BrainExtracts and Plasma Samples at Each Time Point Time Dose PointConcentration Compound Group Tissue Rat ID (hr) (ng/mL) NicotineNicotine Rat Brain 7D 0.5 110 0.4 mg/kg Nicotine Nicotine Rat Brain 7E0.5 71 0.4 mg/kg Nicotine Nicotine Rat Brain 7F 0.5 102 0.4 mg/kgNicotine Nicotine Rat Brain 7G 6 5 0.4 mg/kg Nicotine Nicotine Rat Brain7H 6 <LLQ 0.4 mg/kg Nicotine Nicotine Rat Brain 7I 6 7 0.4 mg/kgNicotine Nicotine Rat Brain 7A 24 5 0.4 mg/kg Nicotine Nicotine RatBrain 7B 24 5 0.4 mg/kg Nicotine Nicotine Rat Brain 7C 24 9 0.4 mg/kgNicotine Nicotine Rat Brain 8D 0.5 117 0.4 mg/kg Nicotine Nicotine RatBrain 8E 0.5 120 0.4 mg/kg Nicotine Nicotine Rat Brain 8F 0.5 123 0.4mg/kg Nicotine Nicotine Rat Brain 8G 6 <LLQ 0.4 mg/kg Nicotine NicotineRat Brain 8H 6 <LLQ 0.4 mg/kg Nicotine Nicotine Rat Brain 8I 6 5 0.4mg/kg Nicotine Nicotine Rat Brain 8A 24 <LLQ 0.4 mg/kg Nicotine NicotineRat Brain 8B 24 7 0.4 mg/kg Nicotine Nicotine Rat Brain 8C 24 <LLQ 0.4mg/kg Anatabine Anatabine Rat Brain 1D 0.5 <LLQ 0.1 mg/kg AnatabineAnatabine Rat Brain 1E 0.5 19 0.1 mg/kg Anatabine Anatabine Rat Brain 1F0.5 21 0.1 mg/kg Anatabine Anatabine Rat Brain 1G 6 3 0.1 mg/kgAnatabine Anatabine Rat Brain 1H 6 <LLQ 0.1 mg/kg Anatabine AnatabineRat Brain 1I 6 <LLQ 0.1 mg/kg Anatabine Anatabine Rat Brain 1A 24 3 0.1mg/kg Anatabine Anatabine Rat Brain 1B 24 <LLQ 0.1 mg/kg AnatabineAnatabine Rat Brain 1C 24 <LLQ 0.1 mg/kg Anatabine Anatabine Rat Brain2D 0.5 34 0.1 mg/kg Anatabine Anatabine Rat Brain 2E 0.5 25 0.1 mg/kgAnatabine Anatabine Rat Brain 2F 0.5 30 0.1 mg/kg Anatabine AnatabineRat Brain 2G 6 5 0.1 mg/kg Anatabine Anatabine Rat Brain 2H 6 4 0.1mg/kg Anatabine Anatabine Rat Brain 2I 6 2 0.1 mg/kg Anatabine AnatabineRat Brain 2A 24 2 0.1 mg/kg Anatabine Anatabine Rat Brain 2B 24 <LLQ 0.1mg/kg Anatabine Anatabine Rat Brain 2C 24 <LLQ 0.1 mg/kg AnatabineAnatabine Rat Brain 3D 0.5 266 0.75 mg/kg Anatabine Anatabine Rat Brain3E 0.5 317 0.75 mg/kg Anatabine Anatabine Rat Brain 3F 0.5 245 0.75mg/kg Anatabine Anatabine Rat Brain 3G 6 17 0.75 mg/kg AnatabineAnatabine Rat Brain 3H 6 27 0.75 mg/kg Anatabine Anatabine Rat Brain 3I6 20 0.75 mg/kg Anatabine Anatabine Rat Brain 3A 24 <LLQ 0.75 mg/kgAnatabine Anatabine Rat Brain 3B 24 <LLQ 0.75 mg/kg Anatabine AnatabineRat Brain 3C 24 <LLQ 0.75 mg/kg Anatabine Anatabine Rat Brain 4D 0.5 3930.75 mg/kg Anatabine Anatabine Rat Brain 4E 0.5 272 0.75 mg/kg AnatabineAnatabine Rat Brain 4F 0.5 279 0.75 mg/kg Anatabine Anatabine Rat Brain4G 6 16 0.75 mg/kg Anatabine Anatabine Rat Brain 4H 6 28 0.75 mg/kgAnatabine Anatabine Rat Brain 4I 6 19 0.75 mg/kg Anatabine Anatabine RatBrain 4A 24 <LLQ 0.75 mg/kg Anatabine Anatabine Rat Brain 4B 24 <LLQ0.75 mg/kg Anatabine Anatabine Rat Brain 4C 24 <LLQ 0.75 mg/kg AnatabineAnatabine Rat Brain 5D 0.5 349 1.0 mg/kg Anatabine Anatabine Rat Brain5E 0.5 338 1.0 mg/kg Anatabine Anatabine Rat Brain 5F 0.5 282 1.0 mg/kgAnatabine Anatabine Rat Brain 5G 6 3 1.0 mg/kg Anatabine Anatabine RatBrain 5H 6 4 1.0 mg/kg Anatabine Anatabine Rat Brain 5I 6 8 1.0 mg/kgAnatabine Anatabine Rat Brain 5A 24 3 1.0 mg/kg Anatabine Anatabine RatBrain 5B 24 2 1.0 mg/kg Anatabine Anatabine Rat Brain 5C 24 <LLQ 1.0mg/kg Anatabine Anatabine Rat Brain 6D 0.5 362 1.0 mg/kg AnatabineAnatabine Rat Brain 6E 0.5 393 1.0 mg/kg Anatabine Anatabine Rat Brain6F 0.5 283 1.0 mg/kg Anatabine Anatabine Rat Brain 6G 6 <LLQ 1.0 mg/kgAnatabine Anatabine Rat Brain 6H 6 8 1.0 mg/kg Anatabine Anatabine RatBrain 6I 6 4 1.0 mg/kg Anatabine Anatabine Rat Brain 6A 24 <LLQ 1.0mg/kg Anatabine Anatabine Rat Brain 6B 24 <LLQ 1.0 mg/kg AnatabineAnatabine Rat Brain 6C 24 <LLQ 1.0 mg/kg Nicotine Nicotine Rat 7A 0.25194 0.4 mg/kg Plasma Nicotine Nicotine Rat 7B 0.25 156 0.4 mg/kg PlasmaNicotine Nicotine Rat 7C 0.25 145 0.4 mg/kg Plasma Nicotine Nicotine Rat7A 0.5 123 0.4 mg/kg Plasma Nicotine Nicotine Rat 7B 0.5 85 0.4 mg/kgPlasma Nicotine Nicotine Rat 7C 0.5 90 0.4 mg/kg Plasma NicotineNicotine Rat 7D 0.5 187 0.4 mg/kg Plasma Nicotine Nicotine Rat 7E 0.5118 0.4 mg/kg Plasma Nicotine Nicotine Rat 7F 0.5 157 0.4 mg/kg PlasmaNicotine Nicotine Rat 7A 1 72 0.4 mg/kg Plasma Nicotine Nicotine Rat 7B1 67 0.4 mg/kg Plasma Nicotine Nicotine Rat 7C 1 68 0.4 mg/kg PlasmaNicotine Nicotine Rat 7A 1.5 33 0.4 mg/kg Plasma Nicotine Nicotine Rat7B 1.5 30 0.4 mg/kg Plasma Nicotine Nicotine Rat 7C 1.5 44 0.4 mg/kgPlasma Nicotine Nicotine Rat 7A 2 21 0.4 mg/kg Plasma Nicotine NicotineRat 7B 2 32 0.4 mg/kg Plasma Nicotine Nicotine Rat 7C 2 21 0.4 mg/kgPlasma Nicotine Nicotine Rat 7A 4 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 7B 4 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 7C 4 <LLQ0.4 mg/kg Plasma Nicotine Nicotine Rat 7A 6 <LLQ 0.4 mg/kg PlasmaNicotine Nicotine Rat 7B 6 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat7C 6 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 7G 6 <LLQ 0.4 mg/kgPlasma Nicotine Nicotine Rat 7H 6 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 7I 6 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 7A 8 <LLQ0.4 mg/kg Plasma Nicotine Nicotine Rat 7B 8 <LLQ 0.4 mg/kg PlasmaNicotine Nicotine Rat 7C 8 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat7A 24 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 7B 24 <LLQ 0.4 mg/kgPlasma Nicotine Nicotine Rat 7C 24 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 8A 0.25 175 0.4 mg/kg Plasma Nicotine Nicotine Rat 8B 0.25145 0.4 mg/kg Plasma Nicotine Nicotine Rat 8C 0.25 184 0.4 mg/kg PlasmaNicotine Nicotine Rat 8A 0.5 111 0.4 mg/kg Plasma Nicotine Nicotine Rat8B 0.5 95 0.4 mg/kg Plasma Nicotine Nicotine Rat 8C 0.5 125 0.4 mg/kgPlasma Nicotine Nicotine Rat 8D 0.5 180 0.4 mg/kg Plasma NicotineNicotine Rat 8E 0.5 157 0.4 mg/kg Plasma Nicotine Nicotine Rat 8F 0.5160 0.4 mg/kg Plasma Nicotine Nicotine Rat 8A 1 67 0.4 mg/kg PlasmaNicotine Nicotine Rat 8B 1 72 0.4 mg/kg Plasma Nicotine Nicotine Rat 8C1 107 0.4 mg/kg Plasma Nicotine Nicotine Rat 8A 1.5 49 0.4 mg/kg PlasmaNicotine Nicotine Rat 8B 1.5 37 0.4 mg/kg Plasma Nicotine Nicotine Rat8C 1.5 64 0.4 mg/kg Plasma Nicotine Nicotine Rat 8A 2 25 0.4 mg/kgPlasma Nicotine Nicotine Rat 8B 2 24 0.4 mg/kg Plasma Nicotine NicotineRat 8C 2 46 0.4 mg/kg Plasma Nicotine Nicotine Rat 8A 4 3 0.4 mg/kgPlasma Nicotine Nicotine Rat 8B 4 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 8C 4 4 0.4 mg/kg Plasma Nicotine Nicotine Rat 8A 6 <LLQ 0.4mg/kg Plasma Nicotine Nicotine Rat 8B 6 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 8C 6 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 8G 6 <LLQ0.4 mg/kg Plasma Nicotine Nicotine Rat 8H 6 <LLQ 0.4 mg/kg PlasmaNicotine Nicotine Rat 8I 6 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat8A 8 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 8B 8 <LLQ 0.4 mg/kgPlasma Nicotine Nicotine Rat 8C 8 <LLQ 0.4 mg/kg Plasma NicotineNicotine Rat 8A 24 <LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 8B 24<LLQ 0.4 mg/kg Plasma Nicotine Nicotine Rat 8C 24 <LLQ 0.4 mg/kg PlasmaAnatabine Anatabine Rat 1A 0.25 24 0.1 mg/kg Plasma Anatabine AnatabineRat 1B 0.25 14 0.1 mg/kg Plasma Anatabine Anatabine Rat 1C 0.25 20 0.1mg/kg Plasma Anatabine Anatabine Rat 1A 0.5 16 0.1 mg/kg PlasmaAnatabine Anatabine Rat 1B 0.5 17 0.1 mg/kg Plasma Anatabine AnatabineRat 1C 0.5 13 0.1 mg/kg Plasma Anatabine Anatabine Rat 1D 0.5 30 0.1mg/kg Plasma Anatabine Anatabine Rat 1E 0.5 32 0.1 mg/kg PlasmaAnatabine Anatabine Rat 1F 0.5 33 0.1 mg/kg Plasma Anatabine AnatabineRat 1A 1 10 0.1 mg/kg Plasma Anatabine Anatabine Rat 1B 1 16 0.1 mg/kgPlasma Anatabine Anatabine Rat 1C 1 11 0.1 mg/kg Plasma AnatabineAnatabine Rat 1A 1.5 7 0.1 mg/kg Plasma Anatabine Anatabine Rat 1B 1.5<LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 1C 1.5 6 0.1 mg/kg PlasmaAnatabine Anatabine Rat 1A 2 6 0.1 mg/kg Plasma Anatabine Anatabine Rat1B 2 8 0.1 mg/kg Plasma Anatabine Anatabine Rat 1C 2 5 0.1 mg/kg PlasmaAnatabine Anatabine Rat 1A 4 3 0.1 mg/kg Plasma Anatabine Anatabine Rat1B 4 3 0.1 mg/kg Plasma Anatabine Anatabine Rat 1C 4 <LLQ 0.1 mg/kgPlasma Anatabine Anatabine Rat 1A 6 <LLQ 0.1 mg/kg Plasma AnatabineAnatabine Rat 1B 6 <LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 1C 6<LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 1G 6 7 0.1 mg/kg PlasmaAnatabine Anatabine Rat 1H 6 4 0.1 mg/kg Plasma Anatabine Anatabine Rat1I 6 4 0.1 mg/kg Plasma Anatabine Anatabine Rat 1A 8 <LLQ 0.1 mg/kgPlasma Anatabine Anatabine Rat 1B 8 <LLQ 0.1 mg/kg Plasma AnatabineAnatabine Rat 1C 8 <LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 1A 24<LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 1B 24 <LLQ 0.1 mg/kgPlasma Anatabine Anatabine Rat 1C 24 <LLQ 0.1 mg/kg Plasma AnatabineAnatabine Rat 2D 0.5 31 0.1 mg/kg Plasma Anatabine Anatabine Rat 2E 0.530 0.1 mg/kg Plasma Anatabine Anatabine Rat 2F 0.5 34 0.1 mg/kg PlasmaAnatabine Anatabine Rat 2G 6 3 0.1 mg/kg Plasma Anatabine Anatabine Rat2H 6 4 0.1 mg/kg Plasma Anatabine Anatabine Rat 2I 6 4 0.1 mg/kg PlasmaAnatabine Anatabine Rat 2A 0.25 15 0.1 mg/kg Plasma Anatabine AnatabineRat 2B 0.25 21 0.1 mg/kg Plasma Anatabine Anatabine Rat 2C 0.25 14 0.1mg/kg Plasma Anatabine Anatabine Rat 2A 0.5 16 0.1 mg/kg PlasmaAnatabine Anatabine Rat 2B 0.5 13 0.1 mg/kg Plasma Anatabine AnatabineRat 2C 0.5 10 0.1 mg/kg Plasma Anatabine Anatabine Rat 2A 1 12 0.1 mg/kgPlasma Anatabine Anatabine Rat 2B 1 12 0.1 mg/kg Plasma AnatabineAnatabine Rat 2C 1 9 0.1 mg/kg Plasma Anatabine Anatabine Rat 2A 1.5 140.1 mg/kg Plasma Anatabine Anatabine Rat 2B 1.5 12 0.1 mg/kg PlasmaAnatabine Anatabine Rat 2C 1.5 7 0.1 mg/kg Plasma Anatabine AnatabineRat 2A 2 8 0.1 mg/kg Plasma Anatabine Anatabine Rat 2B 2 8 0.1 mg/kgPlasma Anatabine Anatabine Rat 2C 2 4 0.1 mg/kg Plasma AnatabineAnatabine Rat 2A 4 3 0.1 mg/kg Plasma Anatabine Anatabine Rat 2B 4 5 0.1mg/kg Plasma Anatabine Anatabine Rat 2C 4 <LLQ 0.1 mg/kg PlasmaAnatabine Anatabine Rat 2A 6 <LLQ 0.1 mg/kg Plasma Anatabine AnatabineRat 2B 6 3 0.1 mg/kg Plasma Anatabine Anatabine Rat 2C 6 <LLQ 0.1 mg/kgPlasma Anatabine Anatabine Rat 2A 8 <LLQ 0.1 mg/kg Plasma AnatabineAnatabine Rat 2B 8 <LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 2C 8<LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 2A 24 <LLQ 0.1 mg/kgPlasma Anatabine Anatabine Rat 2B 24 <LLQ 0.1 mg/kg Plasma AnatabineAnatabine Rat 2C 24 <LLQ 0.1 mg/kg Plasma Anatabine Anatabine Rat 3A0.25 216 0.75 mg/kg Plasma Anatabine Anatabine Rat 3B 0.25 162 0.75mg/kg Plasma Anatabine Anatabine Rat 3C 0.25 223 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3A 0.5 176 0.75 mg/kg Plasma Anatabine AnatabineRat 3B 0.5 176 0.75 mg/kg Plasma Anatabine Anatabine Rat 3C 0.5 190 0.75mg/kg Plasma Anatabine Anatabine Rat 3D 0.5 342 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3E 0.5 271 0.75 mg/kg Plasma Anatabine AnatabineRat 3F 0.5 292 0.75 mg/kg Plasma Anatabine Anatabine Rat 3A 1 153 0.75mg/kg Plasma Anatabine Anatabine Rat 3B 1 146 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3C 1 156 0.75 mg/kg Plasma Anatabine AnatabineRat 3A 1.5 120 0.75 mg/kg Plasma Anatabine Anatabine Rat 3B 1.5 124 0.75mg/kg Plasma Anatabine Anatabine Rat 3C 1.5 136 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3A 2 73 0.75 mg/kg Plasma Anatabine AnatabineRat 3B 2 74 0.75 mg/kg Plasma Anatabine Anatabine Rat 3C 2 104 0.75mg/kg Plasma Anatabine Anatabine Rat 3A 4 29 0.75 mg/kg Plasma AnatabineAnatabine Rat 3B 4 36 0.75 mg/kg Plasma Anatabine Anatabine Rat 3C 4 390.75 mg/kg Plasma Anatabine Anatabine Rat 3A 6 15 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3B 6 14 0.75 mg/kg Plasma Anatabine AnatabineRat 3C 6 13 0.75 mg/kg Plasma Anatabine Anatabine Rat 3G 6 15 0.75 mg/kgPlasma Anatabine Anatabine Rat 3H 6 31 0.75 mg/kg Plasma AnatabineAnatabine Rat 3I 6 20 0.75 mg/kg Plasma Anatabine Anatabine Rat 3A 8 80.75 mg/kg Plasma Anatabine Anatabine Rat 3B 8 11 0.75 mg/kg PlasmaAnatabine Anatabine Rat 3C 8 8 0.75 mg/kg Plasma Anatabine Anatabine Rat3A 24 <LLQ 0.75 mg/kg Plasma Anatabine Anatabine Rat 3B 24 <LLQ 0.75mg/kg Plasma Anatabine Anatabine Rat 3C 24 <LLQ 0.75 mg/kg PlasmaAnatabine Anatabine Rat 4A 0.25 204 0.75 mg/kg Plasma AnatabineAnatabine Rat 4B 0.25 226 0.75 mg/kg Plasma Anatabine Anatabine Rat 4C0.25 207 0.75 mg/kg Plasma Anatabine Anatabine Rat 4A 0.5 166 0.75 mg/kgPlasma Anatabine Anatabine Rat 4B 0.5 229 0.75 mg/kg Plasma AnatabineAnatabine Rat 4C 0.5 175 0.75 mg/kg Plasma Anatabine Anatabine Rat 4D0.5 307 0.75 mg/kg Plasma Anatabine Anatabine Rat 4E 0.5 359 0.75 mg/kgPlasma Anatabine Anatabine Rat 4F 0.5 396 0.75 mg/kg Plasma AnatabineAnatabine Rat 4A 1 146 0.75 mg/kg Plasma Anatabine Anatabine Rat 4B 1207 0.75 mg/kg Plasma Anatabine Anatabine Rat 4C 1 165 0.75 mg/kg PlasmaAnatabine Anatabine Rat 4A 1.5 136 0.75 mg/kg Plasma Anatabine AnatabineRat 4B 1.5 134 0.75 mg/kg Plasma Anatabine Anatabine Rat 4C 1.5 150 0.75mg/kg Plasma Anatabine Anatabine Rat 4A 2 89 0.75 mg/kg Plasma AnatabineAnatabine Rat 4B 2 113 0.75 mg/kg Plasma Anatabine Anatabine Rat 4C 2 970.75 mg/kg Plasma Anatabine Anatabine Rat 4A 4 45 0.75 mg/kg PlasmaAnatabine Anatabine Rat 4B 4 50 0.75 mg/kg Plasma Anatabine AnatabineRat 4C 4 41 0.75 mg/kg Plasma Anatabine Anatabine Rat 4A 6 14 0.75 mg/kgPlasma Anatabine Anatabine Rat 4B 6 23 0.75 mg/kg Plasma AnatabineAnatabine Rat 4C 6 18 0.75 mg/kg Plasma Anatabine Anatabine Rat 4G 6 150.75 mg/kg Plasma Anatabine Anatabine Rat 4H 6 38 0.75 mg/kg PlasmaAnatabine Anatabine Rat 4I 6 16 0.75 mg/kg Plasma Anatabine AnatabineRat 4A 8 10 0.75 mg/kg Plasma Anatabine Anatabine Rat 4B 8 12 0.75 mg/kgPlasma Anatabine Anatabine Rat 4C 8 11 0.75 mg/kg Plasma AnatabineAnatabine Rat 4A 24 <LLQ 0.75 mg/kg Plasma Anatabine Anatabine Rat 4B 24<LLQ 0.75 mg/kg Plasma Anatabine Anatabine Rat 4C 24 <LLQ 0.75 mg/kgPlasma Anatabine Anatabine Rat 5A 0.25 296 1.0 mg/kg Plasma AnatabineAnatabine Rat 5B 0.25 291 1.0 mg/kg Plasma Anatabine Anatabine Rat 5C0.25 270 1.0 mg/kg Plasma Anatabine Anatabine Rat 5A 0.5 288 1.0 mg/kgPlasma Anatabine Anatabine Rat 5B 0.5 264 1.0 mg/kg Plasma AnatabineAnatabine Rat 5C 0.5 265 1.0 mg/kg Plasma Anatabine Anatabine Rat 5D 0.5447 1.0 mg/kg Plasma Anatabine Anatabine Rat 5E 0.5 384 1.0 mg/kg PlasmaAnatabine Anatabine Rat 5F 0.5 366 1.0 mg/kg Plasma Anatabine AnatabineRat 5A 1 257 1.0 mg/kg Plasma Anatabine Anatabine Rat 5B 1 225 1.0 mg/kgPlasma Anatabine Anatabine Rat 5C 1 219 1.0 mg/kg Plasma AnatabineAnatabine Rat 5A 1.5 163 1.0 mg/kg Plasma Anatabine Anatabine Rat 5B 1.5148 1.0 mg/kg Plasma Anatabine Anatabine Rat 5C 1.5 160 1.0 mg/kg PlasmaAnatabine Anatabine Rat 5A 2 121 1.0 mg/kg Plasma Anatabine AnatabineRat 5B 2 129 1.0 mg/kg Plasma Anatabine Anatabine Rat 5C 2 119 1.0 mg/kgPlasma Anatabine Anatabine Rat 5A 4 36 1.0 mg/kg Plasma AnatabineAnatabine Rat 5B 4 51 1.0 mg/kg Plasma Anatabine Anatabine Rat 5C 4 401.0 mg/kg Plasma Anatabine Anatabine Rat 5A 6 20 1.0 mg/kg PlasmaAnatabine Anatabine Rat 5B 6 19 1.0 mg/kg Plasma Anatabine Anatabine Rat5C 6 15 1.0 mg/kg Plasma Anatabine Anatabine Rat 5G 6 26 1.0 mg/kgPlasma Anatabine Anatabine Rat 5H 6 38 1.0 mg/kg Plasma AnatabineAnatabine Rat 5I 6 17 1.0 mg/kg Plasma Anatabine Anatabine Rat 5A 8 81.0 mg/kg Plasma Anatabine Anatabine Rat 5B 8 9 1.0 mg/kg PlasmaAnatabine Anatabine Rat 5C 8 6 1.0 mg/kg Plasma Anatabine Anatabine Rat5A 24 <LLQ 1.0 mg/kg Plasma Anatabine Anatabine Rat 5B 24 <LLQ 1.0 mg/kgPlasma Anatabine Anatabine Rat 5C 24 <LLQ 1.0 mg/kg Plasma AnatabineAnatabine Rat 6A 0.25 293 1.0 mg/kg Plasma Anatabine Anatabine Rat 6B0.25 271 1.0 mg/kg Plasma Anatabine Anatabine Rat 6C 0.25 302 1.0 mg/kgPlasma Anatabine Anatabine Rat 6A 0.5 222 1.0 mg/kg Plasma AnatabineAnatabine Rat 6B 0.5 253 1.0 mg/kg Plasma Anatabine Anatabine Rat 6C 0.5236 1.0 mg/kg Plasma Anatabine Anatabine Rat 6D 0.5 347 1.0 mg/kg PlasmaAnatabine Anatabine Rat 6E 0.5 362 1.0 mg/kg Plasma Anatabine AnatabineRat 6F 0.5 395 1.0 mg/kg Plasma Anatabine Anatabine Rat 6A 1 218 1.0mg/kg Plasma Anatabine Anatabine Rat 6B 1 225 1.0 mg/kg Plasma AnatabineAnatabine Rat 6C 1 244 1.0 mg/kg Plasma Anatabine Anatabine Rat 6A 1.5196 1.0 mg/kg Plasma Anatabine Anatabine Rat 6B 1.5 192 1.0 mg/kg PlasmaAnatabine Anatabine Rat 6C 1.5 211 1.0 mg/kg Plasma Anatabine AnatabineRat 6A 2 147 1.0 mg/kg Plasma Anatabine Anatabine Rat 6B 2 170 1.0 mg/kgPlasma Anatabine Anatabine Rat 6C 2 174 1.0 mg/kg Plasma AnatabineAnatabine Rat 6A 4 73 1.0 mg/kg Plasma Anatabine Anatabine Rat 6B 4 521.0 mg/kg Plasma Anatabine Anatabine Rat 6C 4 57 1.0 mg/kg PlasmaAnatabine Anatabine Rat 6A 6 33 1.0 mg/kg Plasma Anatabine Anatabine Rat6B 6 34 1.0 mg/kg Plasma Anatabine Anatabine Rat 6C 6 21 1.0 mg/kgPlasma Anatabine Anatabine Rat 6G 6 27 1.0 mg/kg Plasma AnatabineAnatabine Rat 6H 6 24 1.0 mg/kg Plasma Anatabine Anatabine Rat 6I 6 181.0 mg/kg Plasma Anatabine Anatabine Rat 6A 8 19 1.0 mg/kg PlasmaAnatabine Anatabine Rat 6B 8 19 1.0 mg/kg Plasma Anatabine Anatabine Rat6C 8 15 1.0 mg/kg Plasma Anatabine Anatabine Rat 6A 24 <LLQ 1.0 mg/kgPlasma Anatabine Anatabine Rat 6B 24 <LLQ 1.0 mg/kg Plasma AnatabineAnatabine Rat 6C 24 <LLQ 1.0 mg/kg Plasma

TABLE 15 Mean Concentrations and Descriptive Statistics of Anatabine andNicotine in Rat Brain Extracts and Plasma Samples at Each Time PointCombined Male and Female Male and Male or Female Female Avg. Conc. Avg.Conc. (ng/ml for (ng/ml for Time plasma and plasma and Point ng/g forng/g for Compound Dose Group Tissue Sex (hr) N = brain) ±STDEV ±SEMbrain) n = stdev sem Nicotine Nicotine Rat Brain male 0.5 3 94.3 20.611.9 107.2 6 19.3 7.9 0.4 mg/kg Nicotine Nicotine Rat Brain male 6 2 6.01.4 1.0 5.7 3 1.2 0.7 0.4 mg/kg Nicotine Nicotine Rat Brain male 24 36.3 2.3 1.3 6.5 4 1.9 1.0 0.4 mg/kg Nicotine Nicotine Rat Brain female0.5 3 120.0 3.0 1.7 0.4 mg/kg Nicotine Nicotine Rat Brain female 6 1 5.0ND ND 0.4 mg/kg Nicotine Nicotine Rat Brain female 24 1 7.0 ND ND 0.4mg/kg Anatabine Anatabine Rat Brain male 0.5 2 20.0 1.4 1.0 25.8 5 6.22.8 0.1 mg/kg Anatabine Anatabine Rat Brain male 6 1 3.0 ND ND 3.5 4 1.30.6 0.1 mg/kg Anatabine Anatabine Rat Brain male 24 1 3.0 ND ND 2.5 20.7 0.5 0.1 mg/kg Anatabine Anatabine Rat Brain female 0.5 3 29.7 4.52.6 0.1 mg/kg Anatabine Anatabine Rat Brain female 6 3 3.7 1.5 0.9 0.1mg/kg Anatabine Anatabine Rat Brain female 24 1 2.0 ND ND 0.1 mg/kgAnatabine Anatabine Rat Brain male 0.5 3 276.0 37.0 21.4 295.3 6 53.321.8 0.75 mg/kg Anatabine Anatabine Rat Brain male 6 3 21.3 5.1 3.0 21.26 5.1 2.1 0.75 mg/kg Anatabine Anatabine Rat Brain male 24 0 <LLQ ND ND<LLQ 0 ND ND 0.75 mg/kg Anatabine Anatabine Rat Brain female 0.5 3 314.767.9 39.2 0.75 mg/kg Anatabine Anatabine Rat Brain female 6 3 21.0 6.23.6 0.75 mg/kg Anatabine Anatabine Rat Brain female 24 0 <LLQ ND ND 0.75mg/kg Anatabine Anatabine Rat Brain male 0.5 3 323.0 35.9 20.7 334.5 644.3 18.1 1.0 mg/kg Anatabine Anatabine Rat Brain male 6 3 5.0 2.6 1.55.4 5 2.4 1.1 1.0 mg/kg Anatabine Anatabine Rat Brain male 24 2 2.5 0.70.5 2.5 2 0.7 0.5 1.0 mg/kg Anatabine Anatabine Rat Brain female 0.5 3346.0 56.7 32.7 1.0 mg/kg Anatabine Anatabine Rat Brain female 6 2 6.02.8 2.0 1.0 mg/kg Anatabine Anatabine Rat Brain female 24 0 <LLQ ND ND1.0 mg/kg Nicotine Nicotine Rat male 0.25 3 165.0 25.7 14.8 166.5 6 20.88.5 0.4 mg/kg Plasma Nicotine Nicotine Rat male 0.5 3 99.3 20.6 11.9104.8 6 17.2 7.0 0.4 mg/kg Plasma Nicotine Nicotine Rat male 0.5 3 154.034.6 20.0 159.8 6 24.1 9.9 0.4 mg/kg Plasma Nicotine Nicotine Rat male 13 69.0 2.6 1.5 75.5 6 15.6 6.4 0.4 mg/kg Plasma Nicotine Nicotine Ratmale 1.5 3 35.7 7.4 4.3 42.8 6 12.5 5.1 0.4 mg/kg Plasma NicotineNicotine Rat male 2 3 24.7 6.4 3.7 28.2 6 9.6 3.9 0.4 mg/kg PlasmaNicotine Nicotine Rat male 4 0 <LLQ ND ND 3.5 2 0.7 0.5 0.4 mg/kg PlasmaNicotine Nicotine Rat male 6 0 <LLQ ND ND <LLQ 0 ND ND 0.4 mg/kg PlasmaNicotine Nicotine Rat male 8 0 <LLQ ND ND <LLQ 0 ND ND! 0.4 mg/kg PlasmaNicotine Nicotine Rat male 24 0 <LLQ ND ND <LLQ 0 ND ND 0.4 mg/kg PlasmaNicotine Nicotine Rat female 0.25 3 168.0 20.4 11.8 108.4 5 83.0 37.10.4 mg/kg Plasma Nicotine Nicotine Rat female 0.5 3 110.3 15.0 8.7 79.712 65.0 18.8 0.4 mg/kg Plasma Nicotine Nicotine Rat female 0.5 3 165.712.5 7.2 95.3 6 77.7 31.7 0.4 mg/kg Plasma Nicotine Nicotine Rat female1 3 82.0 21.8 12.6 50.8 6 37.6 15.3 0.4 mg/kg Plasma Nicotine NicotineRat female 1.5 3 50.0 13.5 7.8 33.6 5 24.4 10.9 0.4 mg/kg PlasmaNicotine Nicotine Rat female 2 3 31.7 12.4 7.2 19.2 6 15.8 6.5 0.4 mg/kgPlasma Nicotine Nicotine Rat female 4 2 3.5 0.7 0.5 3.6 5 0.9 0.4 0.4mg/kg Plasma Nicotine Nicotine Rat female 6 0 <LLQ ND ND 5.5 2 2.1 1.50.4 mg/kg Plasma Nicotine Nicotine Rat female 6 0 <LLQ ND ND 5.5 2 2.11.5 0.4 mg/kg Plasma Nicotine Nicotine Rat female 8 0 <LLQ ND ND 4.0 1ND ND 0.4 mg/kg Plasma Nicotine Nicotine Rat female 24 0 <LLQ ND ND <LLQ0 ND ND 0.4 mg/kg Plasma Anatabine Anatabine Rat male 0.25 3 19.3 5.02.9 18.0 6 4.2 1.7 0.1 mg/kg Plasma Anatabine Anatabine Rat male 0.5 315.3 2.1 1.2 22.9 12 9.4 2.7 0.1 mg/kg Plasma Anatabine Anatabine Ratmale 0.5 3 31.7 1.5 0.9 31.7 6 1.6 0.7 0.1 mg/kg Plasma AnatabineAnatabine Rat male 1 3 12.3 3.2 1.9 8.0 6 5.2 2.1 0.1 mg/kg PlasmaAnatabine Anatabine Rat male 1.5 2 6.5 0.7 0.5 9.2 5 2.8 1.2 0.1 mg/kgPlasma Anatabine Anatabine Rat male 2 3 6.3 1.5 0.9 8.7 6 3.6 1.5 0.1mg/kg Plasma Anatabine Anatabine Rat male 4 2 3.0 0.0 0.0 5.2 5 2.6 1.20.1 mg/kg Plasma Anatabine Anatabine Rat male 6 0 <LLQ ND ND 4.3 6 1.50.6 0.1 mg/kg Plasma Anatabine Anatabine Rat male 6 3 5.0 1.7 1.0 4.5 41.7 0.9 0.1 mg/kg Plasma Anatabine Anatabine Rat male 8 0 <LLQ ND ND<LLQ 0 ND ND 0.1 mg/kg Plasma Anatabine Anatabine Rat male 24 0 <LLQ NDND <LLQ 0 ND ND 0.1 mg/kg Plasma Anatabine Anatabine Rat female 0.25 316.7 3.8 2.2 0.1 mg/kg Plasma Anatabine Anatabine Rat female 0.5 3 13.03.0 1.7 0.1 mg/kg Plasma Anatabine Anatabine Rat female 0.5 3 31.7 2.11.2 0.1 mg/kg Plasma Anatabine Anatabine Rat female 6 3 3.7 0.6 0.3 0.1mg/kg Plasma Anatabine Anatabine Rat female 1 3 11.0 1.7 1.0 0.1 mg/kgPlasma Anatabine Anatabine Rat female 1.5 3 11.0 3.6 2.1 0.1 mg/kgPlasma Anatabine Anatabine Rat female 2 3 6.7 2.3 1.3 0.1 mg/kg PlasmaAnatabine Anatabine Rat female 4 2 4.0 1.4 1.0 0.1 mg/kg PlasmaAnatabine Anatabine Rat female 6 1 3.0 ND ND 0.1 mg/kg Plasma AnatabineAnatabine Rat female 8 0 <LLQ ND ND 0.1 mg/kg Plasma Anatabine AnatabineRat female 24 0 <LLQ ND ND 0.1 mg/kg Plasma Anatabine Anatabine Rat male0.25 3 200.3 33.4 19.3 206.3 6 23.4 9.5 0.75 mg/kg Plasma AnatabineAnatabine Rat male 0.5 3 180.7 8.1 4.7 256.6 12 82.2 23.7 0.75 mg/kgPlasma Anatabine Anatabine Rat male 0.5 3 301.7 36.5 21.1 327.8 6 46.418.9 0.75 mg/kg Plasma Anatabine Anatabine Rat male 1 3 151.7 5.1 3.0162.2 6 23.1 9.4 0.75 mg/kg Plasma Anatabine Anatabine Rat male 1.5 3126.7 8.3 4.8 133.3 6 10.6 4.3 0.75 mg/kg Plasma Anatabine Anatabine Ratmale 2 3 83.7 17.6 10.2 91.7 6 16.1 6.6 0.75 mg/kg Plasma AnatabineAnatabine Rat male 4 3 34.7 5.1 3.0 40.0 6 7.3 3.0 0.75 mg/kg PlasmaAnatabine Anatabine Rat male 6 3 14.0 1.0 0.6 19.3 12 7.8 2.2 0.75 mg/kgPlasma Anatabine Anatabine Rat male 6 3 22.0 8.2 4.7 22.5 6 9.7 4.0 0.75mg/kg Plasma Anatabine Anatabine Rat male 8 3 9.0 1.7 1.0 10.0 6 1.7 0.70.75 mg/kg Plasma Anatabine Anatabine Rat male 24 0 <LLQ ND ND <LLQ 0 NDND 0.75 mg/kg Plasma Anatabine Anatabine Rat female 0.25 3 212.3 11.96.9 0.75 mg/kg Plasma Anatabine Anatabine Rat female 0.5 3 190.0 34.119.7 0.75 mg/kg Plasma Anatabine Anatabine Rat female 0.5 3 354.0 44.725.8 0.75 mg/kg Plasma Anatabine Anatabine Rat female 1 3 172.7 31.218.0 0.75 mg/kg Plasma Anatabine Anatabine Rat female 1.5 3 140.0 8.75.0 0.75 mg/kg Plasma Anatabine Anatabine Rat female 2 3 99.7 12.2 7.10.75 mg/kg Plasma Anatabine Anatabine Rat female 4 3 45.3 4.5 2.6 0.75mg/kg Plasma Anatabine Anatabine Rat female 6 3 18.3 4.5 2.6 0.75 mg/kgPlasma Anatabine Anatabine Rat female 6 3 23.0 13.0 7.5 0.75 mg/kgPlasma Anatabine Anatabine Rat female 8 3 11.0 1.0 0.6 0.75 mg/kg PlasmaAnatabine Anatabine Rat female 24 0 <LLQ ND ND 0.75 mg/kg PlasmaAnatabine Anatabine Rat male 0.25 3 285.7 13.8 8.0 287.2 6 13.4 5.5 1.0mg/kg Plasma Anatabine Anatabine Rat male 0.5 3 272.3 13.6 7.8 319.1 1273.1 21.1 1.0 mg/kg Plasma Anatabine Anatabine Rat male 0.5 3 399.0 42.524.6 383.5 6 35.4 14.5 1.0 mg/kg Plasma Anatabine Anatabine Rat male 1 3233.7 20.4 11.8 231.3 6 15.7 6.4 1.0 mg/kg Plasma Anatabine AnatabineRat male 1.5 3 157.0 7.9 4.6 178.3 6 24.7 10.1 1.0 mg/kg PlasmaAnatabine Anatabine Rat male 2 3 123.0 5.3 3.1 143.3 6 24.3 9.9 1.0mg/kg Plasma Anatabine Anatabine Rat male 4 3 42.3 7.8 4.5 51.5 6 13.25.4 1.0 mg/kg Plasma Anatabine Anatabine Rat male 6 3 18.0 2.6 1.5 24.312 7.4 2.1 1.0 mg/kg Plasma Anatabine Anatabine Rat male 6 3 27.0 10.56.1 25.0 6 7.6 3.1 1.0 mg/kg Plasma Anatabine Anatabine Rat male 8 3 7.71.5 0.9 12.7 6 5.8 2.3 1.0 mg/kg Plasma Anatabine Anatabine Rat male 240 <LLQ ND ND <LLQ 0 ND ND 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 0.25 3 288.7 15.9 9.2 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 0.5 3 237.0 15.5 9.0 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 0.5 3 368.0 24.6 14.2 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 1 3 229.0 13.5 7.8 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 1.5 3 199.7 10.0 5.8 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 2 3 163.7 14.6 8.4 1.0 mg/kg Plasma Anatabine Anatabine Ratfemale 4 3 60.7 11.0 6.3 1.0 mg/kg Plasma Anatabine Anatabine Rat female6 3 29.3 7.2 4.2 1.0 mg/kg Plasma Anatabine Anatabine Rat female 6 323.0 4.6 2.6 1.0 mg/kg Plasma Anatabine Anatabine Rat female 8 3 17.72.3 1.3 1.0 mg/kg Plasma Anatabine Anatabine Rat female 24 0 <LLQ ND ND1.0 mg/kg Plasma

TABLE 16 Dosing solutions Percentage content of Test compound baseInjection Test anatabine or Dose level concentration volume compoundnicotine base (mg/kg) (mg/mL) (mL/kg) Anatabine 41.6 0.10 0.048 5Anatabine 41.6 0.75 0.36 5 Anatabine 41.6 1.5 0.72 5 Nicotine 35.1 0.750.36 5

TABLE 17 Study Outline Observations, body weight and food Dose levelNumber of consumption Test compound Route (mg/kg) animals (M/F)frequency Vehicle i.v. 0.0 5/5 Daily for 14 days Anatabine i.v. 0.10 5/5Daily for 14 days Anatabine i.v. 0.75 5/5 Daily for 14 days Anatabinei.v. 1.5 5/5 Daily for 14 days Nicotine i.v. 1.5 5/5 Not applicableNicotine¹ i.v. 0.75 5/5 Daily for 14 days

TABLE 18 Test Performed and Tissues Collected Parameter Testsperformed/tissues collected Hematology Hematocrit, Hemoglobin, MCH, MCHConcentration, MCV, RBC, Reticulocyte count, Platelet count, WBC, WBCdifferential, blood smear evaluation Clinical A/G ratio (calculated),ALT, Albumin, Alkaline Chemistry phosphatase, AST, Bilirubin, Calcium,Chloride, Cholesterol (total), Creatinine, Globulin (calculated),Glucose, Phosphorus (inorganic), Potassium, Sodium, Total protein, BUNCoagulation Activated partial thromboplastin time, Prothrombin timeUrinalysis Bilirubin, Blood, color and appearance, Glucose, Ketones, pH,Protein, Specific gravity, Urobilinogen, Volume Necropsy Adrenalglands¹, Brain, Heart, Kidneys, Liver, Lungs, Ovaries and Uterus,Pituitary gland¹, Prostate gland, Spleen, Testes, Thymus, Thyroid andParathyroid glands¹, section of small intestines ¹Not weighed; placed incassettes.

TABLE 19 Dosing Solution Analysis Ex- Actual Actual pected Concen-Concentration Dosing Dose Conc. tration relative to Compound Date(mg/kg) (mg/ml) (mg/mL) Expected % Nicotine Jun 16 0.4 0.081 0.096 118.5Anatabine Jun 09 0.1 0.02 0.016 80 Anatabine Jun 09 0.75 0.15 0.127 85Anatabine Jun 09 1.5 0.2 0.239 119.5

TABLE 20 Mean Increase in Body Weights and Daily Food Consumption(descriptive statistics) Number Mean weight p Mean food p Test Dose ofincrease by day Standard (comparison consumption/ Standard (comparisonCompound (mg/kg) Gender animals 14 (g) Deviation to Vehicle) day (g)Deviation to Vehicle) Vehicle — Male 5 130.6 16.8 27.7 2.8 Female 5 49.76.4 20.3 2.7 Anatabine 0.1 Male 5 132.5 17.1 0.864 31.0 4.0 0.001 Female5 39.0 10.3 0.083 20.8 3.6 0.535 Anatabine 0.75 Male 5 111.6 8.9 0.05527.8 3.2 0.936 Female 5 43.1 9.3 0.229 19.7 2.8 0.434 Anatabine 1.5 Male5 137.9 14.0 0.475 30.8 4.0 0.001 Female 5 38.6 13.0 0.125 19.8 3.00.504 Nicotine 0.75 Male 4 98.5 15.8 0.0001 26.4 3.2 0.098 Female 3 40.83.4 0.071 20.6 2.6 0.598

TABLE 21 Mean Organ Weights (descriptive statistics) for Male Animals byTreatment Group Organ Weight (g) Test Dose Small Compound (mg/kg) ThymusHeart Lungs Liver Kidneys Spleen intestine Prostate Testes Brain Vehicle— Mean 0.77 1.66 1.90 15.81  3.53 1.03 0.64 0.49 3.39 2.02 n = 5 Std0.04 0.18 0.21 1.44 0.30 0.24 0.43 0.11 0.07 0.12 Dev Anatabine 0.1 Mean0.75 1.74 1.98 16.81  3.57 0.82 0.66 0.59 3.42 2.15 n = 5 Std 0.04 0.160.22 0.96 0.29 0.11 0.26 0.12 0.24 0.18 Dev p^(a) ns^(b) ns ns ns ns nsns ns ns ns Anatabine 0.75 Mean 0.67 1.43 1.82 14.50  3.15 0.74 0.680.51 3.21 2.07 n = 5 Std 0.22 0.11 0.16 0.50 0.32 0.12 0.41 0.08 0.420.08 Dev p ns 0.04 ns ns ns 0.04 ns ns ns ns Anatabine 1.5 Mean 0.721.52 1.94 16.55  3.45 0.86 0.68 0.47 3.24 1.93 n = 5 Std 0.14 0.06 0.111.55 0.28 0.10 0.22 0.03 0.28 0.14 Dev p ns ns ns ns ns ns ns ns ns nsNicotine 0.75 Mean 0.58 1.25 1.65 12.69  3.03 0.77 0.55 0.36 3.03 1.94 n= 4 Std 0.13 0.11 0.14 1.04 0.13 0.10 0.13 0.09 0.09 0.09 Dev p ns 0.006 ns  0.008  0.017 ns ns ns ns ns ^(a)p, probability relative toVehicle control; ^(b)ns, not significant

TABLE 22 Mean Organ Weights (descriptive statistics) for Female Animalsby Treatment Group Organ Weight (g) Test Dose Small Ovaries/ Compound(mg/kg) Thymus Heart Lungs Liver Kidneys Spleen intestine uterus BrainVehicle — Mean 0.69 1.27 1.52 10.94  2.34 0.61 0.82 1.10 1.93 n = 5 StdDev 0.10 0.09 0.13 1.18 0.40 0.09 0.39 0.53 0.15 Anatabine 0.1 Mean 0.641.13 1.41 10.84  2.18 0.65 0.65 1.14 1.86 n = 5 Std Dev 0.10 0.14 0.171.38 0.18 0.10 0.15 0.45 0.06 p^(a) ns^(b) ns ns ns ns ns ns ns nsAnatabine 0.75 Mean 0.56 1.11 1.45 10.42  2.30 0.60 0.75 1.58 1.90 n = 5Std Dev 0.04 0.11 0.12 1.09 ns 0.09 0.38 1.20 0.13 p  0.026  0.033 ns nsns ns ns ns ns Anatabine 1.5 Mean 0.57 1.00 1.46 10.04  2.28 0.60 0.701.03 1.95 n = 5 Std Dev 0.05 0.09 0.14 1.16 0.29 0.08 0.23 0.24 0.08 pns  0.001 ns ns ns ns ns ns ns Nicotine 0.75 Mean 0.50 0.99 1.32 9.592.31 0.56 0.36 1.28 1.86 n = 3 Std Dev 0.03 0.14 0.14 0.47 0.03 0.170.07 0.34 0.08 p  0.022  0.013 ns ns ns ns ns ns ns ^(a)p, probabilityrelative to Vehicle control ^(b)ns, not significant

TABLE 23A Hematology Parameters (descriptive statistics) (Part 1) byTreatment Group and Gender PLATELET Treatment WBC × RBC × HGB MCV MCHRETICULOCYTE COUNT × Group Gender 10³/μL 10⁶/μL g/dL HCT % fL pg MCHC %COUNT % 10³/μL Vehicle M n 5 5 5 5 5 5 5 5 4 Mean 10.5 7.3 15.2 45.462.2 20.7 33.4 6.1 1287.3 Std 1.4 0.2 0.5 1.5 1.5 0.6 0.4 1.0 210.8 DevF N 5 5 5 5 5 5 5 5 5 Mean 9.3 7.8 16.4 47.3 61.0 21.0 34.5 5.0 1198.4Std 2.8 0.7 1.7 4.7 1.2 0.6 0.8 1.1 200.2 Dev Anatabine M n 5 5 5 5 5 55 5 5 0.1 mg/kg Mean 15.6 7.4 15.8 47.1 63.4 21.2 33.5 5.5 1248.6 Std4.7 0.4 1.2 2.9 1.8 0.6 0.9 0.5 358.1 Dev p^(a) ns^(b) ns ns ns ns ns nsns ns F n 5 5 5 5 5 5 5 5 3 Mean 9.3 7.8 15.6 46.4 60.0 20.2 33.7 4.5997.3 Std 3.4 0.7 1.0 3.2 2.0 0.8 0.3 1.5 165.8 Dev p ns ns ns ns ns ns0.042^(c) ns ns Anatabine M n 5 5 5 5 5 5 5 5 4 0.75 mg/kg Mean 12.1 7.515.6 45.8 61.4 20.9 34.0 4.4 1325.8 Std 5.7 0.7 1.5 4.0 1.5 0.8 0.7 0.6193.7 Dev p ns ns ns ns ns ns ns 0.012^(c) ns F n 5 5 5 5 5 5 5 5 5 Mean10.3 7.5 15.4 45.2 59.8 20.4 34.1 3.3 1269.6 Std 4.0 0.3 0.5 1.5 2.3 0.80.3 0.9 356.4 Dev p ns ns ns ns ns ns ns 0.022^(c) ns

TABLE 23B Hematology Parameters (descriptive statistics) (Part 1) byTreatment Group and Gender - cont'd PLATELET Treatment WBC × RBC × HGBMCV MCH RETICULOCYTE COUNT × Group Gender 10³/μL 10⁶/μL g/dL HCT % fL pgMCHC % COUNT % 10³/μL Anatabine M n 5 5 5 5 5 5 5 5 5  1.5 mg/kg Mean13.1 7.5 15.4 46.1 62.0 20.6 33.4 4.2 1222.5 Std 3.1 0.2 0.6 2.2 1.9 0.50.4 0.8 248.4 Dev p ns ns ns ns ns ns ns 0.011^(c) ns F n 5 5 5 5 5 5 55 5 Mean 9.2 7.7 15.2 45.4 58.8 19.6 33.4 3.2 1127.4 Std 2.5 0.4 0.7 2.70.8 0.4 0.6 0.9 503.7 Dev p ns ns ns ns 0.011^(c) 0.002^(c) 0.036^(c)0.021^(c) ns Nicotine M n 4 4 4 4 4 4 4 4 4 0.75 mg/kg Mean 11.4 7.615.8 46.6 61.5 20.9 34.0 5.2 1355.8 Std 3.2 0.5 0.7 2.4 1.0 0.6 0.5 0.883.0 Dev p ns ns ns ns ns ns ns ns ns F n 3 3 3 3 3 3 3 3 2 Mean 10.28.0 16.0 46.7 58.7 19.9 34.2 5.1 1363.0 Std 3.1 0.5 0.7 2.2 1.2 0.5 0.20.7 248.9 Dev p ns ns ns ns 0.038^(c) 0.038^(c) ns ns ns ^(a)p,probability relative to Vehicle control ^(b)ns, not significant ^(c)Meanwithin normal range

TABLE 24 Hematology Parameters (descriptive statistics) (Part 2) byTreatment Group and Gender Treatment NEUTROPHIL Group Gender SEG %LYMPHOCYTE % MONOCYTE % EOSINOPHIL % B

Vehicle M n 5 5 5 5

Mean 8.8 89.6 1.6 0.0

Std Dev 2.2 2.3 1.5 0.0

F N 5 5 5 5

Mean 12.6 85.2 2.2 0.0

Std 2.6 2.9 0.4 0.0

Anatabine M n 5 5 5 5

 0.1 mg/kg Mean 8.6 89.2 2.0 0.2

Std Dev 3.6 2.9 1.0 0.4

p^(a) ns^(b) ns ns ns

F n 5 5 5 5

Mean 8.0 90.2 1.8 0.0

Std Dev 1.9 1.9 0.8 0.0

p ns ns ns ns

Anatabine M n 5 5 5 5

0.75 mg/kg Mean 9.8 88.8 1.4 0.0

Std Dev 2.5 2.2 0.5 0.0

p ns ns ns ns

F n 5 5 5 5

Mean 8.6 90.6 0.8 0.0

Std Dev 2.3 2.6 0.8 0.0

p ns ns ns ns

Anatabine M n 5 5 5 5

 1.5 mg/kg Mean 14.6 83.8 1.6 0.0

Std Dev 7.7 8.0 0.9 0.0

p ns ns ns ns

F n 5 5 5 5

Mean 12.6 86.6 0.8 0.0

Std Dev 4.4 3.8 0.8 0.0

p ns ns ns ns

Nicotine M n 4 4 4 4

0.75 mg/kg Mean 11.8 85.8 2.5 0.0

Std Dev 3.3 4.2 1.0 0.0

p ns ns ns ns

F n 3 3 3 3

Mean 12.7 86.3 1.0 0.0

Std Dev 2.1 3.1 1.0 0.0

p ns ns ns ns   ^(a)p, probability relative to Vehicle control ^(b)ns,not significant

indicates data missing or illegible when filed

TABLE 25 Coagulation Parameters (descriptive statistics) by TreatmentGroup and Gender ACTIVATED PARTIAL THROM- PROTHROMBIN TreatmentBOPLASTIN TIME TIME Group Gender (seconds) (seconds) Vehicle M n 5 5Mean 32.0 12.9 Std Dev 2.2 0.5 F n 5 5 Mean 35.4 12.7 Std Dev 4.1 0.3Anatabine M n 5 5 0.1 Mean 32.4 12.8 mg/kg Std Dev 3.3 0.7 p^(a)  ns^(b)ns F n 5 5 Mean 29.4 12.1 Std Dev 3.4 0.4 p ns ns Anatabine M n 5 5 0.75Mean 38.7 13.3 mg/kg Std Dev 9.1 2.6 p ns ns F n 5 5 Mean 33.3 14.1 StdDev 2.8 5.5 p ns ns Anatabine M n 5 5 1.5 Mean 30.6 13.2 mg/kg Std Dev3.1 0.4 p ns ns F n 5 5 Mean 32.5 13.3 Std Dev 2.9 0.2 p ns ns NicotineM n 4 4 0.75 Mean 16.3 13.6 mg/kg Std Dev 1.1 0.6 p <0.001^(c) ns F n 22 Mean 16.9 14.1 Std Dev 2.6 0.2 p 0.002^(c) ns ^(a)p, probabilityrelative to Vehicle control ^(b)ns, not significant ^(c)Mean withinnormal range

TABLE 26A Clinical Chemistry Parameters (descriptive statistics)(Part 1) by Treatment Group and Gender ALK TOT TOT DIR TreatmentPHOSPHATASE ALT AST ALBUMIN PROTEIN GLOBULIN BILIRUBIN BILIRUBIN BUNGroup Gender IU/L IU/L IU/L g/dL g/dL g/dL mg/dL mg/dL mg/dL Vehicle M n5 5 5 5 5 5 5 5 5 Mean 370.80 59.40 99.00 3.12 5.62 2.50 0.00 0.00 18.60Std 72.47 2.07 22.86 0.04 0.04 0.00 0.00 0.00 1.14 Dev F N 5 5 5 5 5 5 55 5 Mean 230.20 58.20 80.80 3.40 6.24 2.84 0.00 0.00 18.20 Std 54.564.44 11.32 0.07 0.09 0.11 0.00 0.00 4.44 Dev Anatabine M n 5 5 5 5 5 5 55 5 0.1 mg/kg Mean 407.40 70.60 96.00 3.24 6.10 2.86 0.00 0.00 18.00 Std145.89 17.77 7.75 0.15 0.23 0.18 0.00 0.00 2.55 Dev p^(a) ns^(b) ns nsns 0.002^(c) 0.002^(c) ns ns ns F n 5 5 5 5 5 5 5 5 5 Mean 248.40 49.6077.00 3.62 6.64 3.02 0.00 0.00 19.80 Std 101.28 9.63 7.42 0.11 0.22 0.130.00 0.00 1.10 Dev p ns ns ns 0.005^(c) 0.005^(c) 0.049^(c) ns ns nsAnatabine M n 5 5 5 5 5 5 5 5 5 0.75 mg/kg Mean 370.80 66.80 89.60 3.286.04 2.76 0.02 0.02 16.60 Std 74.89 14.64 14.12 0.13 0.24 0.11 0.04 0.043.36 Dev p ns ns ns 0.032^(c) 0.005^(c) 0.001^(c) ns ns ns F n 5 5 5 5 55 5 5 5 Mean 158.00 54.60 73.20 3.52 6.38 2.86 0.00 0.00 15.40 Std 45.275.90 14.75 0.08 0.16 0.13 0.00 0.00 0.55 Dev p ns ns ns 0.040^(c) ns nsns ns ns

TABLE 26B Clinical Chemistry Parameters (descriptive statistics)(Part 1) by Treatment Group and Gender - cont'd ALK TOT TOT DIRTreatment PHOSPHATASE ALT AST ALBUMIN PROTEIN GLOBULIN BILIRUBINBILIRUBIN Group Gender IU/L IU/L IU/L g/dL g/dL g/dL mg/dL mg/dL BUNmg/dL Anatabine M n 5 5 5 5 5 5 5 5 5 1.5 mg/kg Mean 411.40 70.40 97.003.32 6.00 2.68 0.00 0.00 17.20 Std 133.64 20.61 26.88 0.13 0.25 0.130.00 0.00 1.30 Dev p ns ns ns 0.012^(c) 0.011^(c) 0.015^(c) ns ns ns F n5 5 5 5 5 5 5 5 5 Mean 194.00 49.20 76.60 3.48 6.36 2.88 0.02 0.02 16.20Std 58.97 6.18 9.21 0.15 0.28 0.16 0.04 0.04 2.17 Dev p ns ns ns ns nsns ns ns ns Nicotine M n 4 4 4 4 4 4 4 4 4 0.75 mg/kg Mean 291.00 55.7582.25 3.08 6.00 2.93 0.05 0.00 17.50 Std 51.59 8.46 7.63 0.05 0.16 0.170.06 0.00 1.73 Dev p ns ns ns ns 0.001^(c) 0.001^(c) ns ns ns F n 3 3 33 3 3 3 3 3 Mean 188.67 68.33 103.00 3.30 6.50 3.20 0.10 0.03 19.00 Std74.33 24.83 29.05 0.00 0.10 0.10 0.00 0.06 1.73 Dev p ns ns ns ns0.009^(c) 0.004^(c) ns ns ns ^(a)p, probability relative to Vehiclecontrol ^(b)ns, not significant ^(c)Mean within normal range

TABLE 27A Clinical Chemistry Parameters (descriptive statistics) (Part2) by Treatment Group and Gender CREAT- CHOLES- PHOSPHO- Treatment ININETEROL GLUCOSE CALCIUM RUS CHLORIDE POTASSIUM SODIUM A/G Group Gendermg/dL mg/dL mg/dL mg/dL mg/dL mEq/L mEq/L mEq/L RATIO Vehicle M n 5 5 55 5 5 5 5 5 Mean 0.36 60.00 222.00 12.12 10.82 98.60 6.30 145.40 1.22Std 0.05 4.06 47.00 0.31 0.51 1.52 0.29 1.14 0.04 Dev F n 5 5 5 5 5 5 55 5 Mean 0.42 67.40 198.20 11.66 9.06 99.80 5.92 145.60 1.18 Std 0.0411.48 13.03 0.34 0.61 0.45 0.50 0.55 0.08 Dev Anatabine M n 5 5 5 5 5 55 5 5 0.1 mg/kg Mean 0.36 67.20 219.00 12.00 10.82 98.00 6.40 146.201.14 Std 0.05 8.35 23.73 0.39 0.54 1.00 0.40 1.48 0.09 Dev p^(a) ns^(b)ns ns ns ns ns ns ns ns F n 5 5 5 5 5 5 5 5 5 Mean 0.44 76.40 207.6011.72 8.08 100.20 5.82 146.80 1.22 Std 0.05 11.63 24.11 0.58 0.48 2.170.65 1.30 0.04 Dev p ns ns ns ns ns ns ns ns ns Anatabine M n 5 5 5 5 55 5 5 5 0.75 mg/kg Mean 0.36 62.80 202.00 12.04 10.92 98.60 6.12 147.801.20 Std 0.05 6.38 25.25 0.38 0.85 1.14 0.45 1.48 0.00 Dev p ns ns ns nsns ns ns 0.021^(c) ns F n 5 5 5 5 5 5 5 5 5 Mean 0.44 69.80 220.80 11.688.64 98.00 5.88 145.00 1.24 Std 0.05 9.88 21.73 0.29 1.22 2.00 0.30 1.220.05 Dev p ns ns ns ns ns ns ns ns ns

TABLE 27B Clinical Chemistry Parameters (descriptive statistics) (Part2) by Treatment Group and Gender - cont'd CREAT- CHOLES- PHOSPHO-Treatment ININE TEROL GLUCOSE CALCIUM RUS CHLORIDE POTASSIUM SODIUM A/GGroup Gender mg/dL mg/dL mg/dL mg/dL mg/dL mEq/L mEq/L mEq/L RATIOAnatabine M n 5 5 5 5 5 5 5 5 5 1.5 mg/kg Mean 0.36 62.40 205.60 11.8811.00 99.80 6.02 147.80 1.24 Std 0.05 4.39 6.11 0.51 0.83 0.84 0.77 1.300.05 Dev p ns ns ns ns ns ns ns 0.015^(c) ns F n 5 5 5 5 5 5 5 5 5 Mean0.40 70.00 188.40 11.36 8.24 100.80 5.74 147.20 1.24 Std 0.00 9.92 9.070.35 0.59 1.92 0.59 0.84 0.05 Dev p ns ns ns ns ns ns ns 0.007^(c) nsNicotine M n 4 4 4 4 4 4 4 4 4 0.75 mg/kg Mean 0.35 61.00 201.00 11.0510.38 99.75 6.20 146.75 1.05 Std 0.06 8.49 10.42 0.06 0.58 0.96 0.500.96 0.06 Dev p ns ns ns <0.001^(c) ns ns ns ns 0.002^(c) F n 3 3 3 3 33 3 3 3 Mean 0.43 65.00 238.67 11.03 8.37 98.67 6.27 145.00 1.03 Std0.06 14.93 53.72 0.21 1.02 1.53 0.50 1.73 0.06 Dev p ns ns ns ns ns nsns ns 0.038^(c) ^(a)p, probability relative to Vehicle control ^(b)ns,not significant ^(c)Mean within normal range

TABLE 28A Dosing Calculations and Body Weights, days 1-5 (anatabine)Dose day 1 day 2 day 3 day 4 day 5 B.W. volume time B.W. B.W. B.W. B.W.B.W. Group Rat M/F (g) (mL) of dosing (g) (g) (g) (g) (g) A-1 1 M 2501.25 10:39 258.0 270.0 280.3 296.0 306.6 vehicle 2 M 228 1.15 10:41238.0 251.0 257.8 273.7 286.0 5 mL/kg 3 M 235 1.18 10:43 241.0 250.0260.2 278.0 287.0 A-2 4 M 224 1.13 10:44 230.0 239.0 247.6 262.6 267.0 5M 236 1.18 10:45 241.0 253.1 261.7 281.0 289.0 A-3 6 F 207 1.03 10:49210.2 220.5 218.1 224.2 227.0 7 F 221 1.1 10:50 221.9 222.0 225.1 229.2235.7 8 F 209 1.05 10:51 210.0 214.0 216.9 219.5 220.0 A-4 9 F 201 110:51 200.0 200.1 205.0 216.7 212.0 10 F 211 1.05 10:52 208.4 215.0216.1 227.9 225.0 B-1 1 M 237 1.18 10:48 245.0 257.0 270.0 286.0 296.5Anatabine 2 M 227 1.13 10:49 233.7 235.1 251.0 270.0 273.8 0.1 mg/kg 3 M230 1.15 10:50 235.0 231.0 252.0 271.2 278.5 B-2 4 M 243 1.23 10:52243.5 253.5 259.4 280.5 288.3 5 M 235 1.18 10:55 239.9 247.3 256.6 273.7286.6 B-3 6 F 226 1.13 10:56 223.0 223.9 230.8 242.3 246.9 7 F 212 1.0510:57 211.1 215.1 213.2 222.4 226.4 8 F 207 1.03 10:58 207.0 208.1 209.1220.7 219.3 B-4 9 F 205 1.03 10:58 201.0 208.8 209.1 211.4 221.0 10 F215 1.08 10:59 210.9 212.8 219.3 224.7 229.5 Dose day 1 day 2 day 3 day4 day 4 B.W. volume B.W. B.W. B.W. B.W. B.W. Group Rat M/F (g) (mL) time(g) (g) (g) (g) (g) C-1 1 M 239 1.2 10:58 242.7 248.9 261.1 275.7 282.3Anatabine 2 M 241 1.2 11:00 251.4 259.7 269.1 286.0 287.6 0.75 mg/kg 3 M229 1.15 11:02 231.9 240.0 252.0 268.0 269.9 C-2 4 M 223 1.13 11:04226.8 232.1 243.0 256.3 262.0 5 M 240 1.2 11:06 239.8 247.2 256.1 271.2275.7 C-3 6 F 214 1.08 11:01 208.9 206.2 214.0 230.0 225.4 7 F 206 1.0311:02 207.7 210.0 214.0 214.7 219.3 8 F 215 1.08 11:03 219.1 225.5 224.8232.4 237.1 C-4 9 F 207 1.03 11:05 196.7 210.0 213.6 222.1 220.8 10 F212 1.05 11:06 199.5 210.1 210.8 220.0 227.6 D-1 1 M 230 1.15 11:07234.0 240.4 258.4 244.4 286.3 Anatabine 2 M 248 1.25 11:21 242.6 254.0267.9 255.1 268.1 1.5 mg/kg 3 M 228 1.15 11:23 231.0 240.3 252.5 247.3269.8 D-2 4 M 239 1.2 11:26 245.3 257.0 272.5 290.2 295.8 5 M 227 1.1511:28 227.8 237.3 250.1 262.0 270.5 D-3 6 F 216 1.08 11:08 213.9 212.0220.0 226.2 228.0 7 F 206 1.03 11:09 204.0 206.2 210.3 216.8 217.5 8 F219 1.1 11:20 219.6 221.6 224.3 234.7 230.9 D-4 9 F 231 1.15 11:22 229.5233.9 237.0 248.1 247.5 10 F 206 1.03 11:23 206.1 208.6 211.4 221.8218.9

TABLE 28B Dosing Calculations and Body Weights, days 6-12 (anatabine)day day day day 6 day 7 day 8 day 9 10 11 12 M/ B.W. B.W. B.W. B.W. B.W.B.W. B.W. Group Rat F (g) (g) (g) (g) (g) (g) (g) A-1 1 M 308 317.0332.0 338.0 348.7 364.2 369.5 vehicle 2 M 283.7 300.0 310.0 315.0 327.2342.6 342.6 5 mL/kg 3 M 287.9 300.0 314.0 317.0 332.0 349.1 354.1 A-2 4M 268.8 273.5 286.0 286.9 296.1 312.7 316.7 5 M 294.6 301.1 315.0 315.2332.3 339.7 351.0 A-3 6 F 228.2 231.7 235.5 237.4 246.7 253.8 248.9 7 F235.3 236.8 260.8 249.8 252.8 261.3 256.3 8 F 221.9 225.9 226.4 230.1236.4 248.0 240.9 A-4 9 F 216 217.4 218.0 224.8 228.5 237.1 238.8 10 F232.4 232.5 233.0 238.3 241.9 256.7 256.9 B-1 1 M 301.8 318.2 327.0336.8 346.4 365.7 359.9 Anatabine 2 M 278 293.8 302.0 303.4 312.9 331.0320.0 0.1 mg/kg 3 M 284.3 297.6 309.0 310.0 319.9 343.8 341.9 B-2 4 M288.3 301.2 310.0 318.7 322.3 346.9 347.3 5 M 219.6 300.7 311.0 317.4330.4 348.8 360.9 B-3 6 F 241.1 246.5 252.0 255.1 261.9 274.8 277.2 7 F235.5 226.4 232.0 239.9 234.5 238.5 246.3 8 F 220.1 221.7 227.0 224.1226.0 233.9 242.0 B-4 9 F 218.8 222.1 223.0 236.0 232.5 245.6 240.0 10 F222.9 232.1 235.0 232.0 233.7 245.4 241.6 C-1 1 M 282.4 294.5 300.0307.6 317.2 334.6 327.6 Anatabine 2 M 287.6 302.9 310.6 319.8 331.9339.8 325.4 0.75 mg/kg 3 M 268.2 281.8 293.4 298.8 307.9 329.4 322.5 C-24 M 268.2 274.1 284.2 296.2 303.8 316.1 324.8 5 M 281.3 287.1 292.0298.5 306.8 321.9 331.1 C-3 6 F 224.4 227.4 232.0 237.3 239.3 250.9249.7 7 F 217.8 223 220.0 226.3 232.2 239.1 233.5 8 F 236.2 243.2 243.0247.6 252.7 268.8 259.6 C-4 9 F 214.7 222 224.6 229.1 230.9 240.9 241.610 F 221.4 219.3 227.4 230.6 233.5 244.1 247.9 D-1 1 M 279.1 292 300.0302.1 317.1 333.0 341.1 Anatabine 2 M 296.9 305.6 319.0 323.1 331.8359.6 360.3 1.5 mg/kg 3 M 280.4 288.2 298.4 303.8 318.3 335.4 327.9 D-24 M 302.3 316.7 326.0 337.3 347.0 369.5 380.4 5 M 274.8 283.5 297.0301.9 310.0 332.6 336.3 D-3 6 F 221.2 229 229.6 232.8 232.8 242.1 236.97 F 204.6 208.1 216.4 218.7 229.0 233.0 227.4 8 F 229.3 235.7 244.0243.9 252.1 259.7 257.1 D-4 9 F 246 249.9 256.7 258.3 260.9 266.9 276.310 F 216.9 224 225.0 225.8 234.5 243.5 240.9

TABLE 28C Dosing Calculations and Body Weights, days 13-14 (anatabine)day 13 day 14 Group Rat M/F B.W. (g) B.W. (g) A-1 1 M 379.1 389.0vehicle 2 M 349 363.0 5 mL/kg 3 M 356 377.0 A-2 4 M 317 325.0 5 M 356371.9 A-3 6 F 258 265.2 7 F 249.8 268.2 8 F 245.6 252.7 A-4 9 F 235245.8 10 F 253 265.7 B-1 1 M 367 391.0 Anatabine 2 M 331 347.3 0.1 mg/kg3 M 349 368.8 B-2 4 M 334.4 353.5 5 M 360 373.8 B-3 6 F 271.8 272.7 7 F244 248.5 8 F 241 243.9 B-4 9 F 242.1 255.6 10 F 244 239.2 C-1 1 M 335.6351.9 Anatabine 2 M 338 357.9 0.75 mg/kg 3 M 330 345.1 C-2 4 M 326 339 5M 326 335.9 C-3 6 F 248 251.5 7 F 237.2 242.8 8 F 268 274.1 C-4 9 F 234250.7 10 F 243 250.6 D-1 1 M 339.8 359.8 Anatabine 2 M 370 389.7 1.5mg/kg 3 M 340 357.1 D-2 4 M 379 399.9 5 M 337 355 D-3 6 F 242.4 249.9 7F 223 224.4 8 F 257 264.7 D-4 9 F 275.8 283.1 10 F 240.3 248.8

TABLE 28D Dosing Calculations and Body Weights, days 1-5 (nicotine) Doseday 1 day 2 day 3 day 4 day 5 volume B.W. B.W. B.W. B.W. B.W. Group RatM/F B.W. (g) (mL) time (g) (g) (g) (g) (g) E-1 1 M 218 1.1 8:45 228239.1 245.1 263.4 269.1 Nicotine 2 M 218 1.1 8:48 223 229.5 241.1 257.6260.7 0.75 mg/kg 3 M 207 1.03 8:50 219 229.1 238.4 252.9 258.7 E-2 4 M214 1.08 8:51 5 M 221 1.1 8:53 227 234.9 243 260.5 272.1 E-3 6 F 1870.93 8:55 191.6 190.5 198 207.8 212.3 7 F 195 0.98 8:57 8 F 193 0.988:59 E-4 9 F 207 1.05 9:01 206.1 213.4 217.1 223.8 226.3 10 F 192 0.959:03 192.8 195.7 199.1 205.6 206.4

TABLE 28E Dosing Calculations and Body Weights, days 6-12 (nicotine) dayday day day 6 day 7 day 8 day 9 10 11 12 M/ B.W. B.W. B.W. B.W. B.W.B.W. B.W. Group Rat F (g) (g) (g) (g) (g) (g) (g) E-1 1 M 270 288 285.6285.6 301 300.1 303 Nicotine 2 M 262.8 277.8 278 274.6 283.4 291.5 287.30.75 mg/kg 3 M 259 279.9 284 274.9 286.1 292.2 290.7 E-2 4 M 5 M 275.4295.8 293.7 303.5 314.2 317.7 329.5 E-3 6 F 207 213 218 219.1 221.8222.8 232.1 7 F 8 F E-4 9 F 228.9 240.1 237.4 236.4 240.1 244.5 248.9 10F 205.5 218.3 217.4 213.2 220.5 226 227.7

TABLE 28F Dosing Calculations and Body Weights, days 13-14 (nicotine)day 13 day 14 Group Rat M/F B.W. (g) B.W. (g) E-1 1 M 312.3 316.1Nicotine 2 M 292.4 297.6 0.75 mg/kg 3 M 299.4 305 E-2 4 M 5 M 330 339.2E-3 6 F 232.6 230.4 7 F 8 F E-4 9 F 251.8 249 10 F 227.3 229

TABLE 29A Average Daily Food Consumption per Rat (grams) Anatabine A -Vehicle B - 0.1 mg/kg C - 0.75 mg/kg D - 1.5 mg/kg Date cage# # of ratsMale Female Male Female Male Female Male Female day 1 1 3 25.1 14.1 25.816.4 23.9 17.1 22.7 16.1 2 2 21.1 15.4 28.0 14.4 19.2 17.1 21.4 13.6 day2 1 3 27.4 16.3 33.8 20.2 26.3 22.5 24.2 20.5 2 2 24.5 20.4 29.1 20.429.5 11.3 30.2 19.8 day 3 1 3 25.4 16.8 24.8 19.4 28.1 21.0 30.1 19.6 22 25.3 20.3 22.0 18.2 26.3 17.4 31.2 20.9 day 4 1 3 26.8 17.6 34.1 23.228.3 21.0 22.1 20.8 2 2 26.4 20.2 28.4 18.0 29.8 18.7 30.0 21.6 day 5 13 28.5 17.2 30.6 22.4 24.4 19.1 30.0 18.5 2 2 28.3 22.4 28.6 21.4 27.021.7 29.0 18.5 day 6 1 3 26.7 20.6 33.6 26.8 25.6 18.8 33.6 14.2 2 226.0 19.2 28.0 18.2 29.5 16.4 35.4 18.4 day 7 1 3 30.1 21.6 35.7 21.729.0 24.0 34.1 21.2 2 2 27.9 20.5 31.8 22.4 31.5 17.4 33.5 28.8 day 8 13 33.2 23.7 33.2 26.5 31.3 23.2 31.7 22.7 2 2 31.5 23.8 31.9 21.3 32.622.8 34.4 19.8 day 9 1 3 29.1 24.1 35.5 21.1 29.1 23.7 33.9 21.7 2 227.7 24.9 36.8 23.6 30.3 23.0 34.5 23.1 day 10 1 3 30.4 22.3 34.7 20.428.7 20.0 33.5 21.7 2 2 29.4 20.5 26.7 16.9 28.0 21.0 32.4 21.7 day 11 13 28.0 19.9 29.1 19.0 24.4 20.5 28.3 15.6 2 2 24.4 22.9 30.6 19.1 26.718.6 29.9 19.0 day 12 1 3 27.4 20.3 31.6 27.9 21.7 16.6 30.1 18.4 2 225.6 18.8 34.9 16.7 31.0 20.4 33.1 20.8 day 13 1 3 33.6 22.4 39.9 29.633.9 22.0 36.8 19.6 2 2 30.8 20.9 27.1 19.3 27.2 17.7 34.7 20.5 day 14 13 28.7 20.9 32.3 18.8 27.8 17.6 29.9 17.1 2 2 26.4 19.6 28.8 19.1 26.420.7 31.4 19.2

TABLE 29B Average Daily Food Consumption per Rat (grams) E- Nicotine0.75 mg/kg Males Female Date cage# # of rats grams # of rats grams day 11 3 20.8 1 23.7 2 1 19.3 2 14.8 day 2 1 3 23.5 1 24.9 2 1 26.2 2 18.4day 3 1 3 26.6 1 22.2 2 1 26.2 2 22.3 day 4 1 3 26.2 1 19.4 2 1 23.7 215.8 day 5 1 3 25.1 1 18.7 2 1 21.9 2 16.2 day 6 1 3 23.8 1 20.0 2 125.9 2 17.2 day 7 1 3 26.5 1 19.4 2 1 27.9 2 21.7 day 8 1 3 24.0 1 20.12 1 28.2 2 20.6 day 9 1 3 27.3 1 24.4 2 1 26.1 2 21.5 day 10 1 3 29.6 122.6 2 1 30.9 2 20.4 day 11 1 3 30.1 1 20.4 2 1 29.1 2 20.3 day 12 1 326.5 1 22.5 2 1 23.4 2 21.7 day 13 1 3 31.9 1 23.7 2 1 28.4 2 21.2 day14 1 3 32.7 1 24.4 2 1 26.4 2 19.6

TABLE 30 Hematology/Coagulation Parameters: Normal Ranges in the RatUnit of Measure Range WBC ×10³/μL  3.0-17.0 RBC ×10⁶/μL  5-10 RGB g/dL11-19 HCT % 35-57 MCV fL 46-65 MCH pg 18-23 MCHC g/dL 31-40 RETICULOCYTE%  0-25 COUNT NEUTROPHIL SEG %  7-15 LYMPHOCYTE % 77-89 MONOCYTE % 0-5EOSINOPHIL % 0-4 BASOPHIL % 0-1 PLATELET COUNT ×10³/μL  200-1500 aPTTsec 13.2-22.4 PT sec 11.0-15.6

TABLE 31 Hematology Parameters Hematology Parameters AnatabineRETICULOCYTE PLATELET Animal Dose WBC RBC HGB HCT MCV MCH MCHC COUNTCOUNT ID Sex (mg/kg) ×10³/μL ×10⁶/μL gm/dL % U³ UUG % % ×10³/μL A1 M 09.4 7.33 14.5 43.6 60 19.7 33.1 4.6 1494 A2 M 0 11.8 7.22 15.1 44.9 6220.9 33.6 6.1 1124 A3 M 0 12.2 7.26 15.4 45.5 63 21.2 33.9 6.8 1088 A4 M0 9.9 7.69 15.8 47.8 62 20.5 33 5.9 TNP¹ A5 M 0 9.4 7.13 15.2 45.4 6421.3 33.4 7.3 1443 A6 F 0 5.8 8.4 18.3 51 61 21.7 35.8 5.6 1500 A7 F 011.6 7.2 15.6 45 63 21.6 34.6 3.4 1057 A8 F 0 12 7.35 15.2 44.3 60 20.634.2 6.3 1263 A9 F 0 7 8.71 18.1 53.5 61 20.8 33.8 4.7 986 A10 F 0 10.17.16 14.6 42.7 60 20.4 34.3 5.2 1186 B1 M 0.1 23.5 8.05 17.6 52.1 6521.9 33.8 6.1 701 B2 M 0.1 15 7.38 15.5 45.7 62 21.1 34 5.4 1339 B3 M0.1 11.1 7.4 16.1 47.5 64 21.8 34 4.7 1601 B4 M 0.1 13.2 7.42 15.2 45 6120.5 33.8 5.6 1107 B5 M 0.1 15.4 6.96 14.5 45.3 65 20.8 32 5.9 1495 B6 F0.1 4.7 7.7 15.8 46.7 61 20.5 33.8 4.8 1145 B7 F 0.1 10.7 8.71 17 51.359 19.6 33.2 5.4 TNP¹ B8 F 0.1 8 7.1 14.8 44 62 20.9 33.6 6.1 TNP¹ B9 F0.1 14 7.06 14.6 43.1 61 20.8 34 3.7 1029 B10 F 0.1 9.2 8.22 15.8 46.857 19.2 33.7 2.4 818 C1 M 0.75 9.9 8.23 16.8 49.6 60 20.3 33.8 3.6 1446C2 M 0.75 11.1 7.51 15.8 45.5 61 21 34.7 4.2 1478 C3 M 0.75 22.1 7.6316.8 48.4 63 22 34.7 4.1 1327 C4 M 0.75 7.5 6.23 13.1 39.2 63 21.1 33.54.7 TNP¹ C5 M 0.75 9.9 7.73 15.4 46.3 60 19.9 33.2 5.3 1052 C6 F 0.7513.5 7.42 15 44.7 60 20.2 33.6 3.4 653 C7 F 0.75 14.5 7.78 14.9 43.9 5619.2 34.1 1.8 1475 C8 F 0.75 10.9 7.11 15.1 44.2 62 21.2 34.2 3.2 1304C9 F 0.75 8 7.58 15.6 45.4 60 20.5 34.3 3.8 1540 C10 F 0.75 4.8 7.8116.2 47.6 61 20.8 34.1 4.1 1376 D1 M 1.5 12.4 7.82 15.8 48 62 20.2 32.94.4 TNP2 D2 M 1.5 15.3 7.43 15.4 46.1 62 20.7 33.4 3.3 1350 D3 M 1.5 8.47.49 16.1 48.5 65 21.5 33.1 3.6 1407 D4 M 1.5 13 7.16 14.6 43.1 60 20.433.8 5.1 1274 D5 M 1.5 16.4 7.37 15 44.8 61 20.4 33.6 4.8 859 D6 F 1.56.4 8.17 15.8 47.1 58 19.3 33.6 3.2 1399 D7 F 1.5 7 7.77 15.1 45.9 5919.4 32.8 2.8 1346 D8 F 1.5 12.1 7.65 14.8 44.3 58 19.3 33.4 4.6 1312 D9F 1.5 10.9 8.01 15.9 48.2 60 19.8 32.9 3.4 228 D10 F 1.5 9.5 7.05 14.241.4 59 20.2 34.4 2.1 1352 E1 M 0.75¹ 9.2 7.43 15.2 45.6 61 20.5 33.44.3 1458 E2 M 0.75¹ 13.6 7.61 15.9 46.2 61 20.8 34.4 4.8 1343 E3 M 0.75¹8.2 8.26 16.8 50 61 20.4 33.7 5.6 1366 E5 M 0.75¹ 14.6 7.04 15.3 44.5 6321.7 34.3 6.1 1256 E6 F 0.75¹ 11.2 8.25 16.2 47.7 58 19.6 34 5.8 1539 E9F 0.75¹ 6.7 7.41 15.2 44.2 60 20.5 34.4 4.9 1187 E10 F 0.75¹ 12.7 8.3616.5 48.3 58 19.7 34.1 4.5 TNP² Hematology Parameters Ani- AnatabineNEUTROPHIL LYM- mal Dose SEG PHOCYTE MONOCYTE EOSINOPHIL BASOPHILPLATELET POLY- ANISO- ID Sex (mg/kg) % % % % % EST CHROMASIA CYTOSIS A1M 0 9 90 1 0 0 ADEQUATE SLIGHT SLIGHT A2 M 0 9 87 4 0 0 ADEQUATE SLIGHTSLIGHT A3 M 0 12 88 0 0 0 ADEQUATE SLIGHT SLIGHT A4 M 0 6 93 1 0 0DECREASED SLIGHT SLIGHT A5 M 0 8 90 2 0 0 ADEQUATE SLIGHT SLIGHT A6 F 09 89 2 0 0 INCREASED SLIGHT SLIGHT A7 F 0 12 86 2 0 0 ADEQUATE SLIGHTSLIGHT A8 F 0 14 84 2 0 0 ADEQUATE DNR DNR A9 F 0 12 86 2 0 0 ADEQUATESLIGHT SLIGHT A10 F 0 16 81 3 0 0 ADEQUATE SLIGHT SLIGHT B1 M 0.1 12 871 0 0 ADEQUATE SLIGHT SLIGHT B2 M 0.1 3 94 3 0 0 ADEQUATE SLIGHT SLIGHTB3 M 0.1 7 90 3 0 0 INCREASED SLIGHT SLIGHT B4 M 0.1 10 87 2 1 0ADEQUATE SLIGHT SLIGHT B5 M 0.1 11 88 1 0 0 ADEQUATE SLIGHT SLIGHT B6 F0.1 8 89 3 0 0 ADEQUATE SLIGHT SLIGHT B7 F 0.1 8 90 2 0 0 ADEQUATESLIGHT SLIGHT B8 F 0.1 7 91 2 0 0 DECREASED SLIGHT SLIGHT B9 F 0.1 6 931 0 0 ADEQUATE SLIGHT SLIGHT B10 F 0.1 11 88 1 0 0 ADEQUATE SLIGHTSLIGHT C1 M 0.75 13 86 1 0 0 ADEQUATE SLIGHT SLIGHT C2 M 0.75 10 89 1 00 ADEQUATE SLIGHT SLIGHT C3 M 0.75 6 92 2 0 0 ADEQUATE SLIGHT SLIGHT C4M 0.75 10 89 1 0 0 DECREASED SLIGHT SLIGHT C5 M 0.75 10 88 2 0 0ADEQUATE DNR DNR C6 F 0.75 6 93 1 0 0 ADEQUATE SLIGHT SLIGHT C7 F 0.7512 87 1 0 0 ADEQUATE SLIGHT SLIGHT C8 F 0.75 9 91 0 0 0 ADEQUATE SLIGHTSLIGHT C9 F 0.75 9 89 2 0 0 INCREASED SLIGHT SLIGHT C10 F 0.75 7 93 0 00 ADEQUATE SLIGHT SLIGHT D1 M 1.5 20 77 3 0 0 DECREASED SLIGHT SLIGHT D2M 1.5 6 93 1 0 0 ADEQUATE SLIGHT SLIGHT D3 M 1.5 12 86 2 0 0 ADEQUATESLIGHT SLIGHT D4 M 1.5 25 74 1 0 0 ADEQUATE SLIGHT SLIGHT D5 M 1.5 10 891 0 0 ADEQUATE SLIGHT SLIGHT D6 F 1.5 11 88 1 0 0 ADEQUATE SLIGHT SLIGHTD7 F 1.5 13 87 0 0 0 ADEQUATE SLIGHT SLIGHT D8 F 1.5 20 80 0 0 0ADEQUATE SLIGHT SLIGHT D9 F 1.5 10 89 1 0 0 ADEQUATE SLIGHT SLIGHT D10 F1.5 9 89 2 0 0 ADEQUATE SLIGHT SLIGHT E1 M 0.75¹ 12 86 2 0 0 ADEQUATESLIGHT SLIGHT E2 M 0.75¹ 11 87 2 0 0 ADEQUATE SLIGHT SLIGHT E3 M 0.75¹16 80 4 0 0 ADEQUATE SLIGHT SLIGHT E5 M 0.75¹ 8 90 2 0 0 ADEQUATE SLIGHTSLIGHT E6 F 0.75¹ 15 83 2 0 0 INCREASED SLIGHT SLIGHT E9 F 0.75¹ 12 87 10 0 ADEQUATE SLIGHT SLIGHT E10 F 0.75¹ 11 89 0 0 0 DECREASED SLIGHTSLIGHT ¹Dose is 0.75 mg/kg nicotine ²TNP: Test not performed due to clotin EDTA tube DNR: Did not report - insufficient sample

TABLE 32 Clinical Chemistry Parameters: Normal Ranges in the Rat Unit ofMeasure Range ALKALINE IU/L 160-500 PHOSPHATASE ALT (SGPT) IU/L 35-80AST (SGOT) IU/L 33-53 GLOBULIN g/dL 1.4-5.0 ALBUMIN g/dL 2.9-5.9 TOTALPROTEIN g/dL 4.5-8.4 TOTAL BILIRUBIN mg/dL   0-0.64 BLOOD UREA mg/dL11-23 NITROGEN (BUN) CREATININE mg/dL 0.4-3.8 CHOLESTEROL mg/dL 35-75GLUCOSE mg/dL  80-300 CALCIUM mg/dL  9.1-15.1 PHOSPHORUS mg/dL  4.7-16.0CHLORIDE mEq/L  79-111 POTASSIUM mEq/L 3.6-9.2 SODIUM mEq/L 142-154

TABLE 33 Clinical Chemistry Parameters Clinical Chemistry ParametersAni- Anatabine ALK TOT TOT DIR mal Dose PHOSPHATASE ALT AST ALBUMINPROTEIN GLOBULIN BILIRUBIN BILIRUBIN BUN ID Sex (mg/kg) IU/L IU/L IU/Lg/dL g/dL g/dL mg/dL mg/dL mg/dL A1 M 0 463 62 85 3.1 5.6 2.5 0 0 19 A2M 0 398 59 78 3.1 5.6 2.5 0 0 17 A3 M 0 275 61 96 3.1 5.6 2.5 0 0 19 A4M 0 393 57 137 3.2 5.7 2.5 0 0 18 A5 M 0 325 58 99 3.1 5.6 2.5 0 0 20 A6F 0 248 55 71 3.4 6.4 3 0 0 17 A7 F 0 265 61 81 3.3 6.2 2.9 0 0 14 A8 F0 292 62 75 3.4 6.2 2.8 0 0 20 A9 F 0 176 52 77 3.5 6.2 2.7 0 0 15 A10 F0 170 61 100 3.4 6.2 2.8 0 0 25 B1 M 0.1 470 92 97 3.4 6.3 2.9 0 0 18 B2M 0.1 227 65 99 3.2 5.8 2.6 0 0 18 B3 M 0.1 364 74 93 3.1 5.9 2.8 0 0 21B4 M 0.1 358 44 85 3.1 6.2 3.1 0 0 14 B5 M 0.1 618 78 106 3.4 6.3 2.9 00 19 B6 F 0.1 261 57 78 3.6 6.7 3.1 0 0 21 B7 F 0.1 140 43 69 3.5 6.32.8 0 0 19 B8 F 0.1 209 47 70 3.6 6.7 3.1 0 0 21 B9 F 0.1 412 62 86 3.86.9 3.1 0 0 19 B10 F 0.1 220 39 82 3.6 6.6 3 0 0 19 C1 M 0.75 479 75 1033.4 6.2 2.8 0 0 15 C2 M 0.75 297 57 66 3.1 5.7 2.6 0 0 18 C3 M 0.75 32565 97 3.2 5.9 2.7 0 0 12 C4 M 0.75 337 50 90 3.3 6.1 2.8 0 0 17 C5 M0.75 416 87 92 3.4 6.3 2.9 0.1 0.1 21 C6 F 0.75 123 63 95 3.5 6.3 2.8 00 15 C7 F 0.75 142 49 69 3.6 6.3 2.7 0 0 16 C8 F 0.75 235 55 76 3.4 6.22.8 0 0 15 C9 F 0.75 130 49 54 3.6 6.6 3 0 0 16 C10 F 0.75 160 57 72 3.56.5 3 0 0 15 D1 M 1.5 389 107 144 3.4 6.2 2.8 0 0 18 D2 M 1.5 644 61 833.2 5.7 2.5 0 0 17 D3 M 1.5 304 65 91 3.5 6.3 2.8 0 0 18 D4 M 1.5 357 5877 3.2 5.8 2.6 0 0 18 D5 M 1.5 363 61 90 3.3 6 2.7 0 0 15 D6 F 1.5 18947 78 3.7 6.6 2.9 0 0 18 D7 F 1.5 218 53 82 3.5 6.5 3 0 0 17 D8 F 1.5181 43 70 3.5 6.5 3 0 0 15 D9 F 1.5 272 58 88 3.4 6.3 2.9 0.1 0.1 18 D10F 1.5 110 45 65 3.3 5.9 2.6 0 0 13 E1 M 0.75¹ 241 54 89 3.1 6 2.9 0.1 015 E2 M 0.75¹ 257 59 81 3.1 6.2 3.1 0 0 18 E3 M 0.75¹ 313 45 72 3.1 5.82.7 0 0 19 E5 M 0.75¹ 353 65 87 3 6 3 0.1 0 18 E6 F 0.75¹ 274 97 133 3.36.4 3.1 0.1 0 20 E9 F 0.75¹ 138 54 75 3.3 6.6 3.3 0.1 0.1 17 E10 F 0.75¹154 54 101 3.3 6.5 3.2 0.1 0 20 ¹Dose is 0.75 mg/kg nicotine

Clinical Chemistry Parameters Anatabine CHOLES- PHOS- Animal DoseCREATININE TEROL GLUCOSE CALCIUM PHORUS CHLORIDE POTASSIUM SODIUM A/G IDSex (mg/kg) mg/dL mg/dL mg/dL mg/dL mg/dL mEq/L mEq/L mEq/L RATIO A1 M 00.3 54 183 12.3 10.9 97 6.8 144 1.2 A2 M 0 0.4 62 215 12.1 11 97 6.1 1451.2 A3 M 0 0.4 60 217 12.2 10.8 99 6.2 147 1.2 A4 M 0 0.3 65 302 12.411.4 100 6.3 145 1.3 A5 M 0 0.4 59 193 11.6 10 100 6.1 146 1.2 A6 F 00.4 85 205 11.9 10 100 5.5 145 1.1 A7 F 0 0.4 72 176 11.3 9 99 5.5 1461.1 A8 F 0 0.4 56 206 11.4 9.1 100 5.8 146 1.2 A9 F 0 0.4 64 197 11.68.9 100 6.7 146 1.3 A10 F 0 0.5 60 207 12.1 8.3 100 6.1 145 1.2 B1 M 0.10.4 65 258 12.7 10.3 98 5.9 148 1.2 B2 M 0.1 0.4 64 219 11.8 10.3 97 6.5144 1.2 B3 M 0.1 0.4 75 214 11.9 11.2 99 6.6 146 1.1 B4 M 0.1 0.3 56 19411.8 11.5 97 6.9 147 1 B5 M 0.1 0.3 76 210 11.8 10.8 99 6.1 146 1.2 B6 F0.1 0.4 90 224 12 8.5 99 5.4 147 1.2 B7 F 0.1 0.5 74 170 11.4 8.2 1026.3 148 1.3 B8 F 0.1 0.5 65 227 11.9 7.4 102 5.2 148 1.2 B9 F 0.1 0.4 66220 12.4 8.5 97 5.5 145 1.2 B10 F 0.1 0.4 87 197 10.9 7.8 101 6.7 1461.2 C1 M 0.75 0.4 69 211 12.3 11 98 6.3 148 1.2 C2 M 0.75 0.4 60 22212.2 10.7 99 6.3 146 1.2 C3 M 0.75 0.3 54 219 11.8 10 100 5.4 147 1.2 C4M 0.75 0.3 62 160 11.5 10.6 99 6 150 1.2 C5 M 0.75 0.4 69 198 12.4 12.397 6.6 148 1.2 C6 F 0.75 0.5 66 237 11.8 9.7 97 5.5 145 1.3 C7 F 0.750.4 64 247 11.3 7.7 96 5.9 144 1.3 C8 F 0.75 0.4 63 192 11.6 9.6 99 6145 1.2 C9 F 0.75 0.4 69 211 12.1 9.2 97 5.7 144 1.2 C10 F 0.75 0.5 87217 11.6 7 101 6.3 147 1.2 D1 M 1.5 0.4 57 209 12.2 10.9 99 7.2 146 1.2D2 M 1.5 0.4 68 204 11 9.6 100 5.4 149 1.3 D3 M 1.5 0.4 64 207 12.2 11.699 6.3 148 1.3 D4 M 1.5 0.3 64 196 12.1 11.6 100 5.3 149 1.2 D5 M 1.50.3 59 212 11.9 11.3 101 5.9 147 1.2 D6 F 1.5 0.4 68 196 11.8 8.4 1026.1 148 1.3 D7 F 1.5 0.4 78 173 11.6 8.5 100 6.3 147 1.2 D8 F 1.5 0.4 81192 11.3 7.2 101 5.2 148 1.2 D9 F 1.5 0.4 67 193 11.2 8.6 98 5 147 1.2D10 F 1.5 0.4 56 188 10.9 8.5 103 6.1 146 1.3 E1 M 0.75¹ 0.3 53 199 11.110.5 100 6.7 147 1.1 E2 M 0.75¹ 0.3 71 204 11.1 10.4 99 6 148 1 E3 M0.75¹ 0.4 55 213 11 9.6 99 5.6 146 1.1 E5 M 0.75¹ 0.4 65 188 11 11 1016.5 146 1 E6 F 0.75¹ 0.5 76 299 11.1 8.8 97 6.8 144 1.1 E9 F 0.75¹ 0.471 196 11.2 9.1 99 6.2 144 1 E10 F 0.75¹ 0.4 48 221 10.8 7.2 100 5.8 1471 ¹Dose is 0.75 mg/kg nicotine

TABLE 34 Coagulation Parameters Coagulation Parameters ACTIVE PARTIALPRO- Anatabine THROMBO- THROMBIN Animal Dose PLASTIN TIME TIME ID Sex(mg/kg) seconds seconds A1 M 0 33.5 13.3 A2 M 0 31.7 13.3 A3 M 0 29.612.5 A4 M 0 30.4 12.3 A5 M 0 34.9 13.1 A6 F 0 36.7 12.8 A7 F 0 36.2 12.7A8 F 0 40.6 13.2 A9 F 0 34.5 12.5 A10 F 0 29.2 12.5 B1 M 0.1 34.9 13.6B2 M 0.1 36.4 13.4 B3 M 0.1 29.6 12.5 B4 M 0.1 28.9 12.3 B5 M 0.1 3212.1 B6 F 0.1 31.1 12.3 B7 F 0.1 34.2 11.3 B8 F 0.1 26 12.2 B9 F 0.126.7 12.3 B10 F 0.1 28.9 12.3 C1 M 0.75 39.7 12.4 C2 M 0.75 43.9 12.1 C3M 0.75 27.9 12.1 C4 M 0.75 50.4 17.9 C5 M 0.75 31.7 12.1 C6 F 0.75 31.411.4 C7 F 0.75 32.5 12.1 C8 F 0.75 31.5 11.6 C9 F 0.75 32.7 11.4 C10 F0.75 38.2 23.8 D1 M 1.5 34.1 13.8 D2 M 1.5 33.8 13.1 D3 M 1.5 28.3 12.9D4 M 1.5 27.9 12.9 D5 M 1.5 29.1 13.5 D6 F 1.5 37.2 13.2 D7 F 1.5 31.713.2 D8 F 1.5 29.3 13 D9 F 1.5 32.3 13.6 D10 F 1.5 32 13.3 E1 M 0.75¹ 1513.8 E2 M 0.75¹ 16.3 13.2 E3 M 0.75¹ 17.6 14.2 E5 M 0.75¹ 16.2 13 E6 F0.75¹ 18.7 13.9 E9 F 0.75¹ 15 14.2 E10 F 0.75¹ UNABLE TO UNABLE TOOBTAIN OBTAIN RESULTS DUE TO RESULTS DUE TO FIBRIN CLOTS FIBRIN CLOTS¹Dose is 0.75 mg/kg nicotine

TABLE 35 Urinalysis Results Anat- abine Urinalysis Ani- Dose SPEC URO-mal (mg/ GRAV- PRO- BILIN- ID Sex kg) VOLUME COLOR CLARITY ITY pH TEINGLUCOSE KETONES OGEN BILIRUBIN BLOOD A1 M 0 <0.5 mL YELLOW HAZY 1.046 7TRACE NEGATIVE 1+ NORMAL NEGATIVE NEGA- TIVE A2 M 0 <0.5 mL YELLOW HAZY1.046 7 TRACE NEGATIVE 1+ NORMAL NEGATIVE NEGA- TIVE A3 M 0 <0.5 mLYELLOW HAZY 1.046 7.5 TRACE NEGATIVE 1+ NORMAL 1+ NEGA- TIVE A4 M 0 <0.5mL YELLOW HAZY 1.031 7.5 TRACE NEGATIVE NEGATIVE NORMAL NEGATIVE 2+ A5 M0 <0.5 mL YELLOW HAZY 1.026 7.5 TRACE NEGATIVE NEGATIVE NORMAL NEGATIVETRACE A6 F 0 <0.5 mL YELLOW HAZY 1.034 6.5 TRACE NEGATIVE NEGATIVENORMAL NEGATIVE TRACE A7 F 0 <0.5 mL YELLOW HAZY 1.034 7 TRACE NEGATIVENEGATIVE NORMAL NEGATIVE TRACE A8 F 0 <0.5 mL YELLOW HAZY 1.024 8.5 ANEGATIVE NEGATIVE NORMAL NEGATIVE NEGA- TIVE A9 F 0 <0.5 mL YELLOW HAZY1.021 8 1+ NEGATIVE NEGATIVE NORMAL NEGATIVE NEGA- TIVE A10 F 0 <0.25 mLYELLOW HAZY 1.047 7 A NEGATIVE NEGATIVE NORMAL NEGATIVE TRACE B1 M 0.1<0.5 mL YELLOW HAZY 1.027 8.5 TRACE NEGATIVE 1+ NORMAL NEGATIVE TRACE B2M 0.1 A DNR DNR DNR DNR DNR DNR DNR DNR DNR DNR B3 M 0.1 <0.5 mL YELLOWHAZY 1.039 7.5 TRACE NEGATIVE NEGATIVE NORMAL NEGATIVE TRACE B4 M 0.1<0.5 mL YELLOW HAZY 1.027 7 NEGA- NEGATIVE 1+ NORMAL NEGATIVE NEGA- TIVETIVE B5 M 0.1 <0.5 mL YELLOW HAZY 1.048 7.5 TRACE NEGATIVE 1+ NORMALNEGATIVE 1+ B6 F 0.1 <0.5 mL YELLOW HAZY 1.039 7.5 A NEGATIVE NEGATIVENORMAL NEGATIVE NEGA- TIVE B7 F 0.1 <0.5 mL YELLOW HAZY 1.036 7.5 ANEGATIVE 1+ NORMAL NEGATIVE TRACE B8 F 0.1 <0.5 mL YELLOW HAZY 1.045 7NEGA- NEGATIVE 1+ NORMAL 1+ NEGA- TIVE TIVE B9 F 0.1 0.5 YELLOW HAZY1.017 8 NEGA- NEGATIVE NEGATIVE NORMAL NEGATIVE NEGA- TIVE TIVE B10 F0.1 A DNR DNR DNR DNR DNR DNR DNR DNR DNR DNR C1 M 0.75 No Urine SampleSubmitted C2 M 0.75 <0.5 mL YELLOW HAZY 1.05  7 TRACE NEGATIVE 1+ NORMALNEGATIVE TRACE C3 M 0.75 <0.5 mL YELLOW HAZY 1.051 7 TRACE NEGATIVE 1+NORMAL NEGATIVE NEGA- TIVE C4 M 0.75 <0.5 mL YELLOW HAZY 1.043 8 TRACENEGATIVE NEGATIVE NORMAL 1+ NEGA- TIVE C5 M 0.75 <0.5 mL YELLOW HAZY1.049 7 TRACE NEGATIVE 1+ NORMAL NEGATIVE NEGA- TIVE C6 F 0.75 <0.5 mLYELLOW HAZY 1.016 7.5 A NEGATIVE NEGATIVE NORMAL NEGATIVE 3+ C7 F 0.75<0.5 mL YELLOW HAZY 1.039 6 A NEGATIVE NEGATIVE NORMAL NEGATIVE TRACE C8F 0.75 <0.5 mL YELLOW HAZY 1.036 8 A NEGATIVE 1+ NORMAL NEGATIVE NEGA-TIVE C9 F 0.75 <0.25 mL YELLOW HAZY A DNR DNR NEGATIVE 1+ DNR NEGATIVEDNR C10 F 0.75 <0.5 mL YELLOW HAZY 1.014 8 1+ NEGATIVE NEGATIVE NORMALNEGATIVE 2+ D1 M 1.5 <0.25 mL YELLOW HAZY 1.031 8 A NEGATIVE 1+ NORMALNEGATIVE 2+ D2 M 1.5 <0.5 mL STRAW CLOUDY 1.034 7.5 A NEGATIVE 1+ NORMALNEGATIVE 2+ D3 M 1.5 <0.25 mL YELLOW HAZY 1.034 7.5 A NEGATIVE 1+ NORMALNEGATIVE 2+ D4 M 1.5 <0.5 mL YELLOW HAZY 1.045 7.5 2+ NEGATIVE 1+ NORMALNEGATIVE 2+ D5 M 1.5 <0.5 mL YELLOW HAZY 1.047 8.5 TRACE NEGATIVE 1+NORMAL NEGATIVE NEGA- TIVE D6 F 1.5 <0.5 mL YELLOW HAZY 1.039 8 1+NEGATIVE NEGATIVE NORMAL NEGATIVE TRACE D7 F 1.5 <0.5 mL YELLOW HAZY1.038 8.5 NEGA- NEGATIVE 1+ NORMAL NEGATIVE NEGA- TIVE TIVE D8 F 1.5<0.5 mL YELLOW HAZY 1.039 7 NEGA- NEGATIVE NEGATIVE NORMAL NEGATIVENEGA- TIVE TIVE D9 F 1.5 No Urine Sample Submitted D10 F 1.5 No UrineSample Submitted DNR—did not report - insufficient sample A. Samplequantity was not sufficient for complete testing Urinalysis AnatabineSPEC Animal Dose GRAV- ID Sex (mg/kg) VOLUME COLOR CLARITY ITY pHPROTEIN GLUCOSE KETONES UROBILINOGEN BILI

E1 M 0.75¹ <0.5 mL YELLOW HAZY 1.054 6 NEGATIVE NEGATIVE NEGATIVE NORMALNEG

E2 M 0.75¹ <0.5 mL YELLOW HAZY 1.058 6.5 TRACE NEGATIVE NEGATIVE NORMALNEG

E3 M 0.75¹ No Urine Sample Submitted E5 M 0.75¹ <0.5 mL YELLOW HAZY1.046 7 NEGATIVE NEGATIVE NEGATIVE NORMAL NEG

E6 F 0.75¹ 10 UL YELLOW HAZY 1.047 6.5 NEGATIVE NEGATIVE NEGATIVE NORMALNEG

E9 F 0.75¹ <0.5 mL YELLOW HAZY 1.052 7.5 NEGATIVE NEGATIVE NEGATIVENORMAL NEG

E10 F 0.75¹ No Urine Sample Submitted ¹Dose is 0.75 mg/kg nicotine A.Sample quantity was not sufficient for complete testing; DNR did notreport due to insufficient sample

indicates data missing or illegible when filed

TABLE 36 Tissue Collection Weights (g) Group A: Vehicle (Males) 1 2 3 45 Tissue weights Tissue weights Tissue weights Tissue weights Tissueweights Thymus 0.80 Thymus 0.80 Thymus 0.80 Thymus 0.70 Thymus 0.76Heart 1.65 Heart 1.78 Heart 1.87 Heart 1.39 Heart 1.62 Lungs 2.02 Lungs1.67 Lungs 2.16 Lungs 1.70 Lungs 1.97 Thyroid/ Cass Thyroid/ CassThyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroid parathyroidparathyroid parathyroid parathyroid Liver 17.19  Liver 17.01  Liver15.67  Liver 13.61  Liver 15.58  Adrenals Cass Adrenals Cass AdrenalsCass Adrenals Cass Adrenals Cass Kidneys 3.86 Kidneys 3.51 Kidneys 3.67Kidneys 3.06 Kidneys 3.54 Spleen 1.12 Spleen 0.86 Spleen 1.41 Spleen0.89 Spleen 0.88 Small 0.53 Small 1.4  Small 0.47 Small 0.41 Small 0.41intestine intestine intestine intestine intestine Prostate 0.31 Prostate0.56 Prostate 0.56 Prostate 0.57 Prostate 0.43 Testes 3.40 Testes 3.33Testes 3.31 Testes 3.46 Testes 3.47 Brain 1.82 Brain 2.04 Brain 2.04Brain 2.04 Brain 2.14 Pituitary Cass Pituitary cass Pituitary cassPituitary Cass Pituitary Cass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow✓ Group A Vehicle (Females) 6 7 8 9 10 Tissue weights Tissue weightsTissue weights Tissue weights Tissue weights Thymus 0.66 Thymus 0.79Thymus 0.78 Thymus 0.55 Thymus 0.66 Heart 1.33 Heart 1.31 Heart 1.34Heart 1.14 Heart 1.22 Lungs 1.67 Lungs 1.60 Lungs 1.36 Lungs 1.41 Lungs1.56 Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/Cass parathyroid parathyroid parathyroid parathyroid parathyroid Liver12.40  Liver 11.24  Liver 10.19  Liver 9.36 Liver 11.49  Adrenals CassAdrenals Cass Adrenals Cass Adrenals Cass Adrenals Cass Kidneys 2.66Kidneys 2.72 Kidneys 2.14 Kidneys 1.75 Kidneys 2.42 Spleen 0.72 Spleen0.68 Spleen 0.56 Spleen 0.50 Spleen 0.61 Small 1.33 Small 0.41 Small0.90 Small 0.44 Small 1.02 intestine intestine intestine intestineintestine Ovaries/ 0.76 Ovaries/ 1.42 Ovaries/ 0.83 Ovaries/ 1.88Ovaries/ 0.61 uterus uterus uterus uterus uterus Brain 1.87 Brain 2.06Brain 1.85 Brain 2.12 Brain 1.76 Pituitary cass Pituitary cass Pituitarycass Pituitary cass Pituitary cass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓Marrow ✓ Group B: Anatabine 0.1 mg/kg (Males) 1 2 3 4 5 Tissue weightsTissue weights Tissue weights Tissue weights Tissue weights Thymus 0.74Thymus 0.74 Thymus 0.76 Thymus 0.71 Thymus 0.81 Heart 1.71 Heart 1.59Heart 1.97 Heart 1.60 Heart 1.85 Lungs 2.31 Lungs 1.77 Lungs 2.08 Lungs1.91 Lungs 1.83 Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ CassThyroid/ Cass parathyroid parathyroid parathyroid parathyroidparathyroid Liver 17.92  Liver 15.45  Liver 16.98  Liver 16.32  Liver17.38  Adrenals Cass Adrenals Cass Adrenals Cass Adrenals Cass AdrenalsCass Kidneys 3.55 Kidneys 3.33 Kidneys 3.70 Kidneys 3.27 Kidneys 3.99Spleen 0.91 Spleen 0.66 Spleen 0.82 Spleen 0.93 Spleen 0.76 Small 0.61Small 0.96 Small 0.88 Small 0.50 Small 0.35 intestine intestineintestine intestine intestine Prostate 0.72 Prostate 0.49 Prostate 0.73Prostate 0.53 Prostate 0.48 Testes 3.69 Testes 3.64 Testes 3.14 Testes3.35 Testes 3.29 Brain 2.35 Brain 2.16 Brain 2.24 Brain 2.11 Brain 1.88Pituitary cass Pituitary cass Pituitary cass Pituitary cass Pituitarycass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Group B: Anatabine 0.1mg/kg (Females) 6 7 8 9 10 Tissue weights Tissue weights Tissue weightsTissue weights Tissue weights Thymus 0.68 Thymus 0.59 Thymus 0.49 Thymus0.71 Thymus 0.73 Heart 1.29 Heart 1.12 Heart 0.95 Heart 1.05 Heart 1.25Lungs 1.42 Lungs 1.39 Lungs 1.15 Lungs 1.52 Lungs 1.59 Thyroid/ CassThyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroidparathyroid parathyroid parathyroid parathyroid Liver 11.54  Liver10.09  Liver 9.94 Liver 12.94  Liver 9.67 Adrenals Cass Adrenals CassAdrenals Cass Adrenals Cass Adrenals Cass Kidneys 2.46 Kidneys 2.02Kidneys 2.02 Kidneys 2.14 Kidneys 2.25 Spleen 0.79 Spleen 0.62 Spleen0.51 Spleen 0.67 Spleen 0.65 Small 0.87 Small 0.71 Small 0.55 Small 0.49Small 0.63 intestine intestine intestine intestine intestine Ovaries/0.96 Ovaries/ 1.79 Ovaries/ 0.84 Ovaries/ 1.42 Ovaries/ 0.70 uterusuterus uterus uterus uterus Brain 1.91 Brain 1.89 Brain 1.75 Brain 1.86Brain 1.89 Pituitary cass Pituitary cass Pituitary cass Pituitary cassPituitary cass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Group C:Anatabine 0.75 mg/kg (Males) 1 2 3 4 5 Tissue weights Tissue weightsTissue weights Tissue weights Tissue weights Thymus 1.02 Thymus 0.52Thymus 0.67 Thymus 0.69 Thymus 0.47 Heart 1.52 Heart 1.38 Heart 1.56Heart 1.39 Heart 1.29 Lungs 1.86 Lungs 1.97 Lungs 1.72 Lungs 1.95 Lungs1.58 Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/Cass parathyroid parathyroid parathyroid parathyroid parathyroid Liver14.92  Liver 13.91  Liver 14.70  Liver 14.01  Liver 14.94  Adrenals CassAdrenals Cass Adrenals Cass Adrenals Cass Adrenals Cass Kidneys 3.45Kidneys 2.77 Kidneys 3.49 Kidneys 3.16 Kidneys 2.89 Spleen 0.71 Spleen0.63 Spleen 0.79 Spleen 0.93 Spleen 0.64 Small 0.54 Small 1.41 Small0.56 Small 0.41 Small 0.47 intestine intestine intestine intestineintestine Prostate 0.49 Prostate 0.49 Prostate 0.65 Prostate 0.46Prostate 0.45 Testes 3.19 Testes 3.84 Testes 3.03 Testes 3.28 Testes2.70 Brain 2.01 Brain 2.19 Brain 2.12 Brain 2.00 Brain 2.02 Pituitarycass Pituitary cass Pituitary cass Pituitary cass Pituitary cass Marrow✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Group C: Anatabine 0.75 mg/kg(Females) 6 7 8 9 10 Tissue weights Tissue weights Tissue weights Tissueweights Tissue weights Thymus 0.56 Thymus 0.53 Thymus 0.63 Thymus 0.52Thymus 0.54 Heart 1.09 Heart 1.21 Heart 1.23 Heart 1.03 Heart 0.99 Lungs1.46 Lungs 1.39 Lungs 1.62 Lungs 1.30 Lungs 1.49 Thyroid/ Cass Thyroid/Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroid parathyroidparathyroid parathyroid parathyroid Liver 10.71  Liver 8.65 Liver 11.37 Liver 11.20  Liver 10.19  Adrenals Cass Adrenals Cass Adrenals CassAdrenals Cass Adrenals Cass Kidneys 2.08 Kidneys 2.20 Kidneys 2.68Kidneys 2.18 Kidneys 2.36 Spleen 0.70 Spleen 0.65 Spleen 0.65 Spleen0.51 Spleen 0.49 Small 0.72 Small 0.37 Small 0.85 Small 0.47 Small 1.34intestine intestine intestine intestine intestine Ovaries/ 0.81 Ovaries/1.50 Ovaries/ 0.72 Ovaries/ 1.23 Ovaries/ 3.65 uterus uterus uterusuterus uterus Brain 1.99 Brain 1.93 Brain 1.73 Brain 2.06 Brain 1.81Pituitary cass Pituitary cass Pituitary cass Pituitary cass Pituitarycass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Group D: Anatabine 1.5mg/kg (Males) 1 2 3 4 5 Tissue weights Tissue weights Tissue weightsTissue weights Tissue weights Thymus 0.83 Thymus 0.77 Thymus 0.54 Thymus0.86 Thymus 0.59 Heart 1.50 Heart 1.53 Heart 1.47 Heart 1.61 Heart 1.47Lungs 1.77 Lungs 2.06 Lungs 1.93 Lungs 2.02 Lungs 1.90 Thyroid/ CassThyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroidparathyroid parathyroid parathyroid parathyroid Liver 15.86  Liver17.03  Liver 17.35  Liver 18.27  Liver 14.26  Adrenals Cass AdrenalsCass Adrenals Cass Adrenals Cass Adrenals Cass Kidneys 3.48 Kidneys 3.54Kidneys 3.02 Kidneys 3.79 Kidneys 3.43 Spleen 0.71 Spleen 0.83 Spleen0.86 Spleen 0.97 Spleen 0.92 Small 0.43 Small 0.77 Small 0.56 Small 1.00Small 0.66 intestine intestine intestine intestine intestine Prostate0.50 Prostate 0.45 Prostate Prostate 0.49 Prostate 0.45 Testes 2.78Testes 3.28 Testes 3.51 Testes 3.41 Testes 3.23 Brain 1.75 Brain 1.81Brain 2.02 Brain 2.00 Brain 2.08 Pituitary cass Pituitary cass Pituitarycass Pituitary cass Pituitary cass Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓Marrow ✓ Group D: Anatabine 1.5 mg/kg (Females) 6 7 8 9 10 Tissueweights Tissue weights Tissue weights Tissue weights Tissue weightsThymus 0.59 Thymus 0.63 Thymus 0.52 Thymus 0.61 Thymus 0.51 Heart 1.12Heart 0.88 Heart 1.04 Heart 0.97 Heart 0.98 Lungs 1.29 Lungs 1.46 Lungs1.37 Lungs 1.60 Lungs 1.59 Thyroid/ Cass Thyroid/ Cass Thyroid/ CassThyroid/ Cass Thyroid/ Cass parathyroid parathyroid parathyroidparathyroid parathyroid Liver 9.65 Liver 8.83 Liver 11.46  Liver 11.05 Liver 9.21 Adrenals Cass Adrenals Cass Adrenals Cass Adrenals CassAdrenals Cass Kidneys 2.17 Kidneys 2.08 Kidneys 2.52 Kidneys 2.64Kidneys 1.97 Spleen 0.53 Spleen 0.65 Spleen 0.64 Spleen 0.68 Spleen 0.51Small 0.49 Small 0.60 Small 1.07 Small 0.56 Small 0.77 intestineintestine intestine intestine intestine Ovaries/ 0.84 Ovaries/ 1.20Ovaries/ 0.98 Ovaries/ 1.34 Ovaries/ 0.78 uterus uterus uterus uterusuterus Brain 1.90 Brain 1.91 Brain 1.97 Brain 2.08 Brain 1.91 Pituitarycass Pituitary cass Pituitary cass Pituitary cass Pituitary cass Marrow✓ Marrow ✓ Marrow ✓ Marrow ✓ Marrow ✓ Group E: Nicotine 0.75 mg/kg(Males) 1 2 3 5 Tissue weights Tissue weights Tissue Weights Tissueweights Thymus 0.54 Thymus 0.46 Thymus 0.56 Thymus 0.76 Heart 1.20 Heart1.17 Heart 1.21 Heart 1.42 Lungs 1.84 Lungs 1.49 Lungs 1.62 Lungs 1.66Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroidparathyroid parathyroid parathyroid Liver 11.97  Liver 12.52  Liver12.06  Liver 14.20  Adrenals Cass Adrenals Cass Adrenals Cass AdrenalsCass Kidneys 3.19 Kidneys 3.04 Kidneys 2.87 Kidneys 3.01 Spleen 0.81Spleen 0.62 Spleen 0.78 Spleen 0.86 Small 0.71 Small 0.56 Small 0.53Small 0.40 intestine intestine intestine intestine Prostate 0.41Prostate 0.28 Prostate 0.45 Prostate 0.28 Testes 3.05 Testes 3.13 Testes3.02 Testes 2.92 Brain 2.06 Brain 1.90 Brain 1.84 Brain 1.94 PituitaryCass Pituitary Cass Pituitary Cass Pituitary Cass Marrow ✓ Marrow ✓Marrow ✓ Marrow ✓ Group E: Nicotine 0.75 mg/kg (Females) 6 9 10 Tissueweights Tissue weights Tissue weights Thymus 0.54 Thymus 0.48 Thymus0.48 Heart 1.09 Heart 1.06 Heart 0.83 Lungs 1.20 Lungs 1.48 Lungs 1.28Thyroid/ Cass Thyroid/ Cass Thyroid/ Cass parathyroid parathyroidparathyroid Liver 9.48 Liver 10.11  Liver 9.18 Adrenals Cass AdrenalsCass Adrenals Cass Kidneys 2.34 Kidneys 2.29 Kidneys 2.29 Spleen 0.46Spleen 0.76 Spleen 0.46 Small 0.41 Small 0.40 Small 0.28 intestineintestine intestine Ovaries/ 1.59 Ovaries/ 0.92 Ovaries/ 1.32 uterusuterus uterus Brain 1.77 Brain 1.93 Brain 1.87 Pituitary Cass PituitaryCass Pituitary Cass Marrow ✓ Marrow ✓ Marrow ✓

TABLE 37 Dosing solutions Test Test compound compound Percentage Doseconcentra- concentra- Injection Test content of level tion (total) tion(base) volume compound anatabine (mg/kg) (mg/mL) (mg/mL) (mL/kg)Anatabine 5.18 0.20 0.772 0.04 5 Anatabine 5.18 2.0 7.72 0.4 5

TABLE 38 Dosing Test Concentration # of Dosing times compound Route Sexmg/kg/dose animals (minutes) Anatabine p.o. M 0.2 4 0, 240, 480 F 0.2 4M 2.0 4 F 2.0 4

TABLE 39 Blood Collection Times Blood Test Concentration # of collectioncompound Route Sex mg/kg/dose animals (minutes) Anatabine p.o. M 0.2 430, 60, 235 F 0.2 4 (pre-dose), 270, M 2.0 4 300, 475 (pre- F 2.0 4dose), 540, 600, 720, 1440

TABLE 40 Calibration Curve Concentrations nominal concentration (nM)stock concentration (μM) 5000 250 1667 83.3 555.5 27.8 185.2 9.3 61.73.1 20.6 1.0 6.9 0.34 2.3 0.11 0.76 0.038 0.25 0.013

TABLE 41 LC/MS/MS ionization conditions and identity of parent andproduct ions. Pre- Prod- Collision Polariza- cursor uct energy CompoundMW tion m/z m/z (V) Anatabine 160.2 Positive 161.1 115.1 28(R,S)-Antabine- 164.24 Positive 165.1 148.1 20 2,4,5,6-d₄

TABLE 42 Limits of Detection and Calibration Curves Lower Limit of UpperLimit of Limit of Detection Quantitation Quantitation Sample (LOD)(ng/mL) (LLQ) (ng/mL) (ULQ) (ng/mL) Anatabine in 0.37 1.1 ≧801 ratplasma

TABLE 43 Dosing Solution Analysis Expected Actual Actual Concen- Concen-Concentration Dose tration tration relative to Compound (mg/kg) (mg/mL)(mg/mL) Expected (%) anatabine 0.2 0.04 0.025 63% anatabine 2.0 0.40.335 84%

TABLE 44 Comparison of pharmacokinetic parameters (T_(max), C_(p, max)and C_(p, min)) between male and female rats in each of the twotreatment groups. Anatabine (0.6 mg/kg) Anatabine (6.0 mg/kg) MaleFemale Male Female Parameter n Mean SD n Mean SD p n Mean SD n Mean SD pT_(max (1)) (hr) 4 0.75 0.29 4 0.63 0.25 0.537 4 0.63 0.25 4 0.50 0.000.356 T_(max (2)) (hr) 4 0.63 0.25 4 0.88 0.25 0.207 4 0.63 0.25 4 0.630.25 1.000 T_(max (3)) (hr) 4 1.00 0 4 1.25 0.50 0.356 4 2.00 1.41 41.25 0.50 0.356 C_(p, max (1)) 4 34.3 2.1 4 38.3 6.1 0.262 4 244 86 4260 35 0.738 (ng/mL) C_(p, max (2)) 4 30.3 3.8 4 31.3 14.2 0.896 4 30553 4 312 77 0.889 (ng/mL) C_(p, max (3)) 3 37.3 8.1 4 35.5 10.6 0.814 4283 94 4 375 123 0.281 (ng/mL) C_(p, min (1)) 3 11.0 2.0 4 10.3 6.40.856 4 75 26 4 52 26 0.254 (ng/mL) C_(p, min (2)) 3 15.3 5.5 4 7.5 1.70.040 4 93 16 4 180 31 0.002 (ng/mL)

TABLE 45 Comparison of pharmacokinetic parameters (C_(p, max) andC_(p, min)) over time for male and female rats in each of the twotreatment groups. Anatabine (0.6 mg/kg) Anatabine (6.0 mg/kg) MaleFemale Male Female Parameter Mean SD p Mean SD p Mean SD p Mean SD pC_(p, max (1)) (ng/mL) 34.3 2.1 0.195 38.3 6.1 0.570 287 11 0.897 259.835.4 0.142 C_(p, max (2)) (ng/mL) 30.3 3.8 31.3 14.2 305 53 312.0 76.8C_(p, max (3)) (ng/mL) 37.3 8.1 35.5 10.6 283 94 374.8 122.9C_(p, min (1)) (ng/mL) 11.0 2.0 0.177 10.3 6.4 0.428 75 26 0.131 51.526.0 0.015 C_(p, min (2)) (ng/mL) 15.3 5.5 7.5 1.7 93 16 180.0 30.7

TABLE 46 Comparison of pharmacokinetic parameters (AUC_(0□□),t_(1/2, 0□4), t_(1/2, terminal), MTT_(0□4) and MAT_(0□4)) between maleand female rats in each of the two treatment groups. Anatabine (0.6mg/kg) Anatabine (6.0 mg/kg) Male Female Male Female Parameter n Mean SDn Mean SD p n Mean SD n Mean SD p AUC_(0□□) (ng · hr/mL) 3 280 102 4 29071 0.880 4 3257 480 4 3735 587 0.255 t_(1/2, 0□□) (hr) 4 2.05 0.43 42.06 1.20 0.986 3 1.76 0.39 4 1.82 0.81 0.918 t_(1/2, terminal) (hr) 31.78 0.68 4 1.80 0.72 0.970 4 5.07 2.05 4 3.99 1.52 0.430 MTT_(0□□) (hr)3 3.17 0.51 4 2.98 1.84 0.873 4 3.18 1.29 4 2.76 1.39 0.668 MAT_(0□□)(hr) 3 0.71 1.34 4 0.53 1.84 0.873 4 0.73 1.29 4 0.30 1.39 0.668

TABLE 47 Comparison of pharmacokinetic parameters (AUC_(0□□),t_(1/2, 0□4), t_(1/2, terminal), MTT_(0□4) and MAT_(0□4)) betweentreatment groups. Anatabine (0.6 mg/kg) Anatabine(6.0 mg/kg) Parameter nMean SD n Mean SD p AUC_(0□□) 7 285 77 8 3496 559 <0.001 (ng · hr/mL)t_(1/2, 0□□) (hr) 8 2.05 0.83 7 1.79 0.62 0.514 t_(1/2, terminal) (hr) 71.79 0.64 8 4.53 1.77 0.002 MTT_(0□□) (hr) 7 3.06 1.34 8 2.97 1.26 0.898MAT_(0□□) (hr) 7 0.61 1.34 8 0.52 1.26 0.898

TABLE 48 Comparison of pharmacokinetic parameters (t_(1/2, 0□4),MTT_(0□4) and MAT_(0□4)) between male and female rats in both treatmentgroups, combined, and all data combined. Male Female Overall Parameter nMean SD n Mean SD p n Mean SD t_(1/2, 0□□) (hr) 7 1.92 0.41 8 1.94 0.960.973 15 1.93 0.73 MTT_(0□□) (hr) 7 3.18 0.96 8 2.87 1.52 0.650 15 3.011.25 MAT_(0□□) (hr) 7 0.72 0.96 8 0.42 1.52 0.650 15 0.56 1.25

TABLE 49 Animal Weights and Dosing Times Dose Time Points for Samples(hrs) - retro-orbital Cmpnd Rat B.W. (g) volume (ml) time 0.5 1 4 (pre)dose (2) 4.5 5 8 (pre) dose (3) 9 10 12 24 1 A 246 1.2 6:06 6:36 7:0610:01 10:06 10:36 11:06 2:01 2:06 3:06 4:06 6:06 6:06 MALE B 231 1.26:07 6:37 7:07 10:02 10:07 10:37 11:07 2:02 2:07 3:07 4:07 6:07 6:07Anatabine C 244 1.2 6:08 6:38 7:08 10:03 10:08 10:38 11:08 2:03 2:083:08 4:08 6:08 6:08 0.2 MPK/dose D 242 1.2 6:09 6:39 7:09 10:04 10:0910:39 11:09 2:04 2:09 3:09 4:09 6:09 6:09 2 A 203 1.0 6:10 6:40 7:1010:05 10:10 10:40 11:10 2:05 2:10 3:10 4:10 6:10 6:10 FEMALE B 200 1.06:11 6:41 7:11 10:06 10:11 10:41 11:11 2:06 2:11 3:11 4:11 6:11 6:11Anatabine C 212 1.1 6:12 6:42 7:12 10:07 10:12 10:42 11:12 2:07 2:123:12 4:12 6:12 6:12 0.2 MPK/dose D 201 1.0 6:13 6:43 7:13 10:08 10:1310:43 11:13 2:08 2:13 3:13 4:13 6:13 6:13 3 A 240 1.2 6:14 6:44 7:1410:09 10:14 10:44 11:14 2:09 2:14 3:14 4:14 6:14 6:14 MALE B 239 1.26:15 6:45 7:15 10:10 10:15 10:45 11:15 2:10 2:15 3:15 4:15 6:15 6:15Anatabine C 241 1.2 6:16 6:46 7:16 10:11 10:16 10:46 11:16 2:11 2:163:16 4:16 6:16 6:16 2.0 MPK/dose D 240 1.2 6:17 6:47 7:17 10:12 10:1710:47 11:17 2:12 2:17 3:17 4:17 6:17 6:17 4 A 208 1.0 6:18 6:48 7:1810:13 10:18 10:48 11:18 2:13 2:18 3:18 4:18 6:18 6:18 FEMALE B 215 1.16:19 6:49 7:19 10:14 10:19 10:49 11:19 2:14 2:19 3:19 4:19 6:19 6:19Anatabine C 207 1.0 6:20 6:50 7:20 10:15 10:20 10:50 11:20 2:15 2:203:20 4:20 6:20 6:20 2.0 MPK/dose D 201 1.00 6:21 6:51 7:21 10:16 10:2110:51 11:21 2:16 2:21 3:21 4:21 6:21 6:21

TABLE 50 Measured Concentrations of Anatabine in Rat Plasma Samples atEach Time Point Time Anatabine Dose Animal Point Concentration (mg/kg)ID Sex (min) (ng/mL) 0.2 1A male 30 34 60 26 235 11 270 35 300 22 475 9540 4 600 <LOQ 720 <LOQ 1440 <LOQ 1B male 30 <LOQ 60 32 235 <LOQ 270 31300 26 475 <LOQ 540 28 600 17 720 5 1440 <LOQ 1C male 30 29 60 34 235 13270 20 300 29 475 18 540 41 600 35 720 12 1440 <LOQ 1D male 30 37 60 24235 9 270 26 300 22 475 19 540 43 600 34 720 19 1440 <LOQ 2A female 3034 60 29 235 4 270 14 300 18 475 7 540 24 600 12 720 18 1440 <LOQ 2Bfemale 30 34 60 33 235 18 270 11 300 31 475 7 540 44 600 18 720 15 1440<LOQ 2C female 30 42 60 47 235 6 270 17 300 25 475 6 540 29 600 20 720 71440 <LOQ 2D female 30 38 60 25 235 13 270 51 300 44 475 10 540 29 60045 720 15 1440 <LOQ 2 3A male 30 298 60 153 235 84 270 131 300 312 47582 540 223 600 269 720 133 1440 12 3B male 30 288 60 106 235 46 270 236300 232 475 79 540 214 600 173 720 401 1440 <LOQ 3C male 30 269 60 272235 63 270 364 300 116 475 97 540 290 600 130 720 137 1440 42 3D male 30116 60 116 235 105 270 309 300 202 475 114 540 173 600 150 720 71 144036 4A female 30 245 60 81 235 75 270 237 300 216 475 144 540 231 600 197720 186 1440 42 4B female 30 78 60 95 235 36 270 324 300 97 475 219 540314 600 207 720 165 1440 8 4C female 30 218 60 127 235 23 270 273 300191 475 178 540 369 600 480 720 244 1440 36 4D female 30 98 60 165 23572 270 350 300 414 475 179 540 474 600 288 720 217 1440 <LOQ

TABLE 51 Mean Concentrations and Descriptive Statistics of Anatabine inPlasma Samples at Each Time Point Combined Male and Female Male and TimeMale or Female Female Dose Point Avg. Conc. Avg. Conc. Group Sex (min) N= (ng/ml) ±SD ±SEM (ng/ml) n = ±SD ±SEM 0.2 male 30 3 33 4.2 2.4 36 74.3 1.6 60 4 30 4.6 2.3 31 8 7.5 2.6 235 3 11 1.6 0.9 10 7 4.7 1.8 270 426 6.9 3.4 26 8 13.3 4.7 300 4 26 3.0 1.5 27 8 7.9 2.8 475 3 18 5.3 3.011 7 5.4 2.0 540 4 38 17.9 8.9 30 8 13.1 4.6 600 3 29 10.4 6.0 26 7 12.34.3 720 3 12 6.5 3.8 13 7 5.2 1.8 1440 0 n/a n/a n/a n/a 0 n/a n/a 0.2female 30 4 37 3.9 2.0 60 4 35 9.7 4.9 235 4 12 6.4 3.2 270 4 26 18.79.4 300 4 34 10.9 5.5 475 4 8 1.7 0.9 540 4 34 8.7 4.4 600 4 28 14.7 7.3720 4 12 4.8 2.4 1440 0 n/a n/a n/a 2 male 30 4 243 85.6 42.8 201 8 90.131.9 60 4 165 76.1 38.0 139 8 60.4 21.3 235 4 72 25.7 12.9 63 8 26.9 9.5270 4 303 100.9 50.5 278 8 76.4 27.0 300 4 183 80.7 40.3 222 8 102.336.2 475 4 97 16.2 8.1 136 8 51.7 18.3 540 4 226 48.3 24.1 286 8 98.734.9 600 4 151 61.7 30.8 237 8 112.2 39.7 720 4 203 146.6 73.3 194 899.1 35.0 1440 3 39 15.9 9.2 29 6 15.5 6.3 2 female 30 4 160 83.8 41.960 4 129 37.3 18.6 235 4 44 25.8 12.9 270 4 316 50.8 25.4 300 4 234133.3 66.6 475 4 192 30.7 15.3 540 4 386 102.1 51.1 600 4 325 131.0 65.5720 4 208 34.7 17.3 1440 3 22 18.6 10.7

EXAMPLE 6 Treatment of Thyroiditis

This example illustrates administering anatabine for treatingthyroiditis. A female patient, aged approximately 52, had been afflictedwith Hashimoto's thyroiditis for approximately 5 years. The patient'scondition had advanced to a state where the treating physicianrecommended a thyroid lobectomy. The patient orally ingested a tabletcontaining about 600 μg anatabine citrate, 20 times daily over a periodof 30 days. At the conclusion of the treatment, inflammation of thethyroid was reduced to normal levels, such that the patient was nolonger in need of a thyroid lobectomy. The patient continued thetreatment for an additional 30 days, after which time the patient'svoice distortion associated with thyroiditis was no longer present.

EXAMPLE 7 Use of Anatabine to Treat Epilepsy and Autism

A 10-year old male patient, who was diagnosed with autism and a seizuredisorder, had brain surgery and began rehabilitation the followingmonth. About 4 months later, in addition to continuing rehabilitation,he began a course of treatment with 1.0 mg of anatabine three times perday. Over the course of 3½ weeks the frequency of the patient's seizuresdecreased from one per day to approximately one per week. The patientalso experienced cognitive benefits beginning approximately one weekafter the start of the anatabine treatment, with noticeable improvementsdaily. These benefits included improved communication and languageskills and the ability to focus.

EXAMPLE 8 Effect of Nicotine and Anatabine on Nicotinic AcetylcholineReceptor Channels In Vitro

This example demonstrates the in vitro effects of nicotine (−) isomerand anatabine racemate (“test articles”) on three cloned human nicotinicacetylcholine receptor (nAChR) channels expressed in mammalian cellsusing a Fluo-8 calcium kit and a Fluorescence Imaging Plate Reader(FLIPR TETRA™) instrument. The following three (3) channels wereevaluated:

-   -   1. nAChR α3/β4 (encoded by the human CHRNA3 and CHRNB4 gene and        stably expressed in CHO cells);    -   2. nAChR α4/β2 (CHRNA4 and CHRNB2 gene and transiently expressed        in HEK293 cells); and    -   3. nAChR α7 (encoded by the human nicotinic α7 gene coexpressed        in CHO cells with the chaperone RIC-3 encoded by the human RIC3        gene).

The ability of each test article to act as an agonist, a positiveallosteric modulator or antagonist of three nAChR receptor channels wasevaluated in the presence of 0.1 μM atropine. Both test articles wereevaluated for responses on each nAChR channel at eight (8)concentrations: 0.3, 1, 3, 10, 30, 100, 300, and 1000 μM (n=4 for eachconcentration). The results are summarized below and detailed in Tables54, 56, and 58. The z-prime factors for each channel are presented inTables 55, 57, and 59.

In the agonist assay, both test articles increased all three nAChRchannel signals in a concentration-dependent manner indicating that thetest articles were agonists of the channels. The nicotine (−) isomershowed the highest agonist activity towards the nAChR α4/β2 channel(EC₅₀=1.302 μM), followed by the nAChR α3/β4 channel (EC₅₀=27.78 μM).The EC₅₀ of nicotine for the nAChR 7 channel could not be determined asmaximal stimulation was not achieved within the range of concentrationstested. The EC₅₀ for the anatabine racemate could only be determined forthe nAChR α4/β2 receptor (EC₅₀=282 μM) as the maximum level ofstimulation was not achieved or could not be determined for the nAChRα3/β4 and nAChR α7 channels. Therefore, anatabine displays full agonistactivity towards the α4/β2 receptor and agonist activity towards theα3/β4 and α7 receptors; however, it was not possible to determine ifanatabine is a partial agonist of the latter two.

In the potentiation assay, the test articles did not increase thesignals with a low dose of Ach stimulation, indicating that they are notpotentiators or allosteric modulators of the channels.

In the antagonist assay, after stimulation with high dose of Ach, thetest articles decreased the Ach-induced signals. However, since the testarticles acted as agonists, the reduction of Ach-induced signals wascaused by the desensitization of the channel themselves, rather than thechannel blockage. Nicotine and anatabine are not considered to beantagonists of these receptors.

Formulations All chemicals used in solution preparations were purchasedfrom Sigma-Aldrich (St. Louis, Mo.) unless otherwise noted and were ofACS reagent grade purity or higher. Stock solutions of test and controlarticles were prepared in dimethyl sulfoxide (DMSO) and stored frozen.Test article and positive control concentrations were prepared freshdaily by diluting stock solutions into the appropriate solutions. Thetest and control article formulations were loaded in a glass-lined,384-well compound plate, and placed in the compound plate wells of aFLIPR TETRA™ (MDS-AT) instrument.

Test Articles The effect of 8 concentrations of each test article wasevaluated (n=4). The sponsor provided the anatabine racemate andnicotine (−) isomer was purchased from Sigma-Aldrich.

Test Amount Concen- Test MW Received Purity trations Article ID Lot(g/mol): (mg or μl) (%) (μM) Anatabine A210192 160.22 2 g 99.5% 0.3, 1,3, (racemate) 10, 30, 100, 300, 1000 Nicotine (−) 1425810V 162.23 25 mL99    0.3, 1, 3, isomer 10, 30, 100, 300, 1000

Positive Control Articles Stock solutions of positive control articleswere prepared in DMSO and stored frozen. Acetylcholine (Ach) wasprepared in distilled H₂O and stored frozen.

TABLE 52 Molecular Rationale for Purpose Name Source Weight selectionpositive PNU-120596 Tocris 311.72 g/mol positive control allostericmodulator of nicotinic receptor channel positive Epibatidine Tocris208.69 g/mol agonist and control potentiator of and nicotinic receptorchannels positive Methyllycaconitine Tocris 874.93 g/mol inhibits α3,control citrate (MLA) α4, and α7 nicotinic receptor channels positiveAcetylcholine Sigma- 181.66 g/mol activates all control (Ach) Aldrichnicotinic receptor channels test article dimethyl sulfoxide Sigma- 78.13 g/mol 0.3% DMSO carrier (DMSO) Aldrich does not affect ionchannel function

Test Systems

Cells were maintained in tissue culture incubators per ChanTest SOP.Stocks were maintained in cryogenic storage.

Cell Culture Procedures

HEK293 or CHO cells were transiently or stably transfected with theappropriate human ion channel cDNAs. Stable transfectants were selectedby coexpression with the antibiotic-resistance gene(s) incorporated intothe expression plasmid(s). Selection pressure was maintained byincluding selection antibiotics in the culture medium. HEK293 cells werecultured in Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12(D-MEM/F-12) supplemented with 10% fetal bovine serum, 100 U/mLpenicillin G sodium, 100 g/mL streptomycin sulfate and appropriateselection antibiotics. CHO cells were cultured in Ham's F-12supplemented with 10% fetal bovine serum, 100 U/mL penicillin G sodium,100 g/mL streptomycin sulfate and appropriate selection antibiotics.

For FLIPR TETRA™ assay, cells were plated in 384-well black wall, flatclear bottom microtiter plates (Type: BD Biocoat Poly-D-Lysine MultiwellCell Culture Plate) at 20,000 to 30,000 cells per well (384-well plate).Cells were incubated at 37° C. overnight or until the cells reached asufficient density in the wells (near confluent monolayer) to use influorescence assays. For α4β2 assay, cells were incubated at 27° C. forat least 7 hours before use.

Test Methods

Experiments were performed with either the FLIPR calcium sensitive dyekit (Fluo-8, ABDbioquest, for nAChR α3/β4 and nAChR α7) or FLIPRmembrane potential kit (Molecular Devices, for nAChR α4/β2) according tothe manufacturer's instructions. Briefly, cells were incubated with 20 ldye for 30 min at 37° C. After dye loading period, for the agonistassay, 5 μl of the test, vehicle, or control articles at concentrationof 5 times of final concentration were applied to the cells withoutstimulation. For the positive allosteric modulation (PAM) and antagonistassay, after test article application, the cells were stimulated witheither low dose (for PAM) or high dose (for antagonist) of Ach.

TABLE 53 designation organism tissue morphology age/stage strain sourcesub-strain source HEK293 H. sapiens kidney; Transformed epithelialembryo ATCC, ChanTest Corp., with adenovirus 5 DNA; Manassas, VACleveland, OH Transfected with human ion channel cDNAs CHO CricetulusOvary; transfected epithelial embryo griseus with human ion channelcDNA(s)

Analysis

Data was stored on the ChanTest computer network (and backed-up nightly)for off-line analysis. Data acquisition was performed via the FLIPRControl software that is supplied with the FLIPR System (MDS-AT) anddata was analyzed using Microsoft Excel 2003 (Microsoft Corp., Redmond,Wash.).

Concentration-response data was fitted to a Hill equation of thefollowing form:

${RESPONSE} = {{Base} + \frac{{Max} - {Base}}{1 + \left( \frac{xhalf}{x} \right)^{rate}}}$

where Base is the response at low concentrations of test article, Max isthe maximum response at high concentrations, xhalf is the EC₅₀ or IC₅₀,the concentration of test article producing either half-maximalactivation or inhibition, and rate is the Hill coefficient. Nonlinearleast squares fits were made assuming a simple one-to-one binding model.

Z-prime factors for the agonist, positive allosteric modulator andantagonist control assays were calculated and are indicative of assayquality. Values above 0.5 represent an excellent assay with clearseparation between positive and negative control responses. Z-primefactors between 0 and 0.5 are marginal, but still useful for screeningpurposes.

1. nAChR α3/β4 Receptor Channel Assay

The ability of both test articles to act as an agonist of nAChR carriedout in the absence of the positive control agonist. The signal elicitedin the presence of the positive control agonist, 30 μM acetylcholine(Ach) was set to 100% and the signal from the vehicle control,HEPES-buffered physiological saline (HBPS) solution was set to 0%. Thetest article results are presented as normalized % activation and areshown in Table 54. Values were considered significant (bold font) if thetest article mean was three or more standard deviations above thevehicle control mean. The concentration-response relationship ofnormalized % activation of Ach is shown in FIG. 24A. The EC₅₀ ofnicotine (−) isomer could be determined (EC₅₀=27.78 μM) and theconcentration-response relationship of normalized % activation for bothtest articles are presented in FIG. 25. Although racemic anatabineshowed agonist activity, the EC₅₀ could not be determined as the maximallevel of stimulation was not achieved within the concentration rangethat was evaluated.

The ability of each test article to act as a positive allostericmodulator of nAChR α3β4 was carried out in the presence of a lowconcentration of the positive control agonist (10 μM Ach) alone. Thesignal elicited in the presence of the positive control agonist andallosteric modulator (10 μM Ach+1 μM epibatidine) was set to 100% andthe signal from the agonist control (10 μM Ach) was set to 0%. The testarticle results are presented as normalized % potentiation and are shownin Table 54. Values were considered significant (bold font) if the testarticle mean was three or more standard deviations above the agonistcontrol mean. Neither nicotine nor anatabine potentiated the activity ofthe nAChR α3/β4 receptor. The concentration-response relationship of thenormalized % potentiation by epibatidine is shown in FIG. 24B.

The ability of each test article to act as an antagonist of nAChR α3/β4was carried out in the presence of a high concentration of the positivecontrol agonist (300 μM Ach) and the positive allosteric modulator (1 μMepibatidine). The signal, elicited in the presence of the positivecontrol agonist and the positive allosteric modulator (300 μM Ach+1 μMepibatidine), was set to 100% and the signal in the presence of thepositive control antagonist (300 μM Ach+1 μM epibatidine+10 μMmethyllycaconitine, MLA) was set to 0. The normalized inhibition of thetest articles are shown in Table 54. Values were considered significant(bold font) if the test article mean was three or more standarddeviations below the positive control agonist plus positive allostericmodulator mean. The concentration-response relationship of normalized %inhibition of MLA is shown in FIG. 24C. The IC₅₀ of both test articlescould be determined (nicotine (−) isomer, IC₅₀ 7.707 μM; racemicanatabine, IC₅₀=34.13 μM) and the concentration-response relationshipsof normalized % inhibition are presented in FIG. 26. It should be notedthat because nicotine and anatabine are both agonists of this receptor,their inhibitory effects are indicative of receptor desensitizationrather than antagonism.

The Z-prime factors for the agonist, positive allosteric modulator andantagonist assays are presented in Table 55 and are indicative of assayquality.

TABLE 54 Effect of the Test Articles on nAChR α3/β4 Channel Normal-Normal- Normal- Test Test ized % ized % ized % Article conc Acti- Poten-Inhi- ID (μM) vation SD tiation SD bition SD Anatabine 0.3 1.32 0.21−1.98 0.90 22.21 4.61 (racemate) 1 −0.01 0.89 −4.08 2.89 21.83 4.51 3−1.53 0.54 −2.88 0.68 27.15 4.93 10 −2.73 0.43 −3.20 1.39 30.61 7.11 304.93 2.71 −8.50 1.70 99.02 3.43 100 10.44 4.31 −9.46 0.68 118.93 4.11300 16.97 4.00 −9.38 0.46 144.56 2.11 1000 22.70 4.38 −9.17 0.47 144.810.13 Nicotine 0.3 0.94 1.49 −1.23 0.69 19.08 6.99 (−) 1 −1.28 1.38 −1.190.51 19.01 2.88 isomer 3 1.11 0.65 −3.92 0.43 37.78 7.71 10 38.17 9.39−5.67 2.19 95.81 9.31 30 122.59 32.46 −9.28 0.93 138.96 0.88 100 201.5062.22 −9.72 0.58 145.26 0.29 300 264.77 37.00 −8.45 0.23 143.89 0.621000 208.23 5.74 −9.57 0.94 142.14 2.34 Note: Bolded values aresignificantly different from the respective control means Foractivation: 3 × SD of vehicle control mean (HBPS) = 4.08; values > 4.08are significant. For positive allosteric modulation: 3 × SD of agonistmean (10 μM Ach) = 9.24; values > 9.24 are significant For inhibition: 3× SD of agonist plus positive allosteric modulator mean (300 μM Ach + 1μM epibatidine) = 10.89; values > 10.89 are significant

TABLE 55 Positive Controls Normalized Channel Test Article ID Signals SDnAChR α3/β4 30 μM Ach 100 5.07 (activation) HBPS 0 1.36 Z Prime = 0.81nAChR α3/β4 10 μM Ach + 1 μM 100 1.12 (potentiation) Epibatidine 10 μMAch 0 3.08 Z Prime = 0.87 nAChR α3/β4 300 μM Ach + 1 μM 0 3.63(inhibition) Epibatidine 300 μM Ach + 1 μM 100 10.09 Epibatidine + 10 μMMLA Z Prime = 0.56

2. nAChR α4/β2 Receptor Channel Assay

The ability of each test article to act as an agonist of the nAChRcarried out in the absence of the positive control agonist. The signalelicited in the presence of the positive control agonist (30 μM Ach) wasset to 100% and the signal from the vehicle control (HBPS) was set to0%. The test article results are presented as normalized % activationand are shown in Table 56. Values were considered significant (boldfont) if the test article mean was three or more standard deviationsabove from the vehicle control mean. The concentration-responserelationship of the normalized % activation of Ach is shown in FIG. 27A.The EC₅₀ of both test articles could be determined (nicotine (−) isomer,EC₅₀=1.302 μM; racemic anatabine, EC₅₀=282 μM) and theconcentration-response relationships of the normalized % activation forthe test articles are presented in FIG. 28. Both test articles are fullagonists of this channel.

The ability of each test article to act as a positive allostericmodulator of nAChR α4/β2 was carried out in the presence of a lowconcentration of the positive control agonist (10 μM Ach) alone. Thesignal elicited in the presence of the positive control agonist andallosteric modulator epibatidine (10 μM Ach+3 μM epibatidine) was set to100% and the signal from the agonist control (10 μM Ach) was set to 0%.The test article results are presented as normalized % potentiation andare shown in Table 56. Values were considered significant (bold font) ifthe test article mean was three or more standard deviations above theagonist mean. The concentration-response relationship of the normalized% potentiation of epibatidine is shown in FIG. 27B. Neither test articlepotentiated the activity of the nAChR α4/β2 receptor.

The ability of each test article to act as an antagonist of nAChR α4/β2was carried out in the presence of a high concentration of the positivecontrol agonist (100 μM Ach) and the positive allosteric modulator, 0.3μM epibatidine. The signal, elicited in the presence of the positivecontrol agonist and the positive allosteric modulator (100 μM Ach+0.3 μMepibatidine), was set to 100% and the signal in the presence of thepositive control antagonist MLA (100 μM Ach+0.3 μM epibatidine+10 μMMLA) was set to 0. The normalized inhibition of the test articles areshown in Table 56. Values were considered significant (bold font) if thetest article mean was three or more standard deviations below thepositive control agonist mean. The concentration-response relationshipof the normalized % inhibition of MLA is shown in FIG. 27C. Theconcentration-response relationships of the normalized % inhibition forthe test articles are presented in FIG. 29. Although both nicotine andanatabine inhibited receptor activity, the IC₅₀s could not be determinedfor either test article since the inhibitions were notconcentration-dependent. Nicotine and anatabine are both agonists ofthis receptor and therefore their inhibitory effects are indicative ofreceptor desensitization rather than antagonism.

The Z-prime factors for the agonist, positive allosteric modulator andantagonist assays are presented in Table 57.

TABLE 56 Effect of the Test Articles on nAChR α4/β2 Channel Normal-Normal- Normal- Test Test ized % ized % ized % Article conc Acti- Poten-Inhi- ID (μM) vation SD tiation SD bition SD Anatabine 0.3 0.28 3.08−18.94 5.64 −20.93 0.41 (racemate) 1 5.36 5.14 −27.03 19.93 49.23 4.59 310.41 8.66 −35.59 2.81 59.57 10.42 10 12.65 1.79 −42.34 7.10 92.94 7.8330 9.07 4.24 −39.48 6.15 84.03 4.80 100 16.96 5.70 −38.34 12.74 97.268.27 300 50.60 2.87 −41.07 9.18 84.96 4.98 1000 85.29 10.49 −35.30 2.5396.88 3.70 Nicotine 0.3 16.27 3.95 −46.00 8.03 85.93 8.84 (−) 1 34.057.15 −46.34 5.03 107.14 6.98 isomer 3 61.88 9.61 −40.54 8.72 85.74 10.2410 74.31 1.54 −42.16 6.73 109.33 9.09 30 75.53 7.12 −43.70 8.78 107.144.81 100 71.02 7.25 −43.40 2.35 91.94 8.93 300 58.23 8.27 −34.56 4.7895.26 3.36 1000 57.05 2.03 −39.66 5.99 108.16 7.40 Note: Bolded valuesare significantly different from the respective control means Foractivation: 3 × SD of vehicle control mean (HBPS) = 12.74; values >12.74 are significant For positive allosteric modulation: 3 × SD ofagonist mean (10 μM Ach) = 20.04; values > 20.04 are significant Forinhibition: 3 × SD of agonist plus positive allosteric modulator mean(100 μM Ach + 0.3 μM epibatidine) = 43.00; values > 43.00 aresignificant

TABLE 57 Positive Controls Normalized Channel Test Article ID Signals SDnAChR α4/β2 30 μM Ach 100 8.87 (activation) HBPS 0 4.25 Z Prime = 0.61nAChR α4/β2 10 μM Ach + 0.3 μM 100 8.24 (potentiation) Epibatidine 10 μMAch 0 6.68 Z Prime = 0.55 nAChR α4/β2 100 μM Ach + 0.3 μM 0 14.33(inhibition) Epibatidine 100 μM Ach + 0.3 μM 100 5.38 Epibatidine + 10μM MLA Z Prime = 0.41

3. nAChR α7 Receptor Channel Assay

The ability of each test article to act as an agonist of nAChR α7receptor channel was carried out in the absence of the positive controlagonist, Ach. The signal elicited in the presence of the positivecontrol agonist and allosteric modulator PNU-120596 (30 μM Ach+10 μMPNU-120596) was set to 100% and the signal from the vehicle control(HBPS) was set to 0%. In the absence of PNU-120596, the nAChR α7receptor became desensitized very quickly before any agonist effect ofAch could be observed. Therefore, the assay of agonist activity foreither Ach or for the test articles was conducted in the presence of thepositive allosteric modulator.

The test article results are presented as the normalized % activationand are shown in Table 58. Values were considered significant (boldfont) if the test article mean was three or more standard deviationsabove the vehicle control mean. The concentration-response relationshipsof the normalized % activation for the test articles are presented inFIG. 31. Although both nicotine and anatabine showed agonist activity,maximal stimulation was not achieved within the range of concentrationstested and therefore, EC₅₀s could not be determined.

The ability of each test article to act as a positive allostericmodulator of nicotinic α7 was carried out in the presence of thepositive control agonist (30 μM Ach) alone. The signal elicited in thepresence of the positive control agonist and allosteric modulatorPNU-120596 (30 μM Ach+10 μM PNU-120596) was set to 100% and the signalfrom the agonist control (30 μM Ach) was set to 0%. The test articleresults are presented as the normalized % potentiation and are shown inTable 58. Values were considered significant and in bold font if thetest article mean was three or more standard deviations above theagonist control mean. The concentration-response relationship of thenormalized % potentiation of PNU-120596 is shown in FIG. 30A. Neithertest article potentiated the activity of the nAChR α7 receptor.

The ability of each test article to act as an antagonist of nAChR α7 wascarried out in the presence of the high concentration of a positivecontrol agonist (300 μM Ach) and the positive allosteric modulator (10μM PNU-120596). The signal, elicited in the presence of the positivecontrol agonist and the positive allosteric modulator (300 μM Ach+10 μMPNU-120596), was set to 100% and the signal in the presence of thepositive control antagonist (300 μM Ach+10 μM PNU-120596+10 μM MLA) wasset to 0. The normalized inhibition of the test articles are shown inTable 58. Values were considered significant (bold font) if the testarticle mean was three or more standard deviations below the positivecontrol agonist plus positive allosteric modulator mean. Theconcentration-response relationship of the normalized % inhibition ofMLA is shown in FIG. 30B. The concentration-response relationships ofthe normalized % inhibition for the test articles are presented in FIG.32. Inhibition was not concentration-dependent and the IC₅₀s could notbe determined for either test article.

The Z-prime factors for the agonist, positive allosteric modulator andantagonist assays are presented in Table 59.

TABLE 58 Effect of the Test Articles on nAChR α7 Channel Normal- Normal-Normal- Test Test ized % ized % ized % Article conc Acti- Poten- Inhi-ID (μM) vation SD tiation SD bition SD Anatabine 0.3 −1.81 0.31 −0.940.09 22.38 2.91 (racemate) 1 0.34 0.42 −1.05 0.06 22.23 9.43 3 0.78 0.43−0.82 0.07 45.19 5.32 10 1.65 0.57 −0.51 0.24 33.42 4.55 30 2.27 0.31−0.57 0.11 22.88 8.05 100 5.69 0.45 −0.64 0.04 21.99 8.18 300 14.45 2.30−0.74 0.09 7.51 5.17 1000 60.41 5.29 −1.05 0.15 10.84 4.92 Nicotine 0.3−1.03 1.21 −0.95 0.07 2.78 7.04 (−) 1 0.15 0.31 −1.03 0.11 11.83 7.05isomer 3 0.72 0.45 −0.81 0.14 41.24 9.79 10 2.44 0.64 −0.61 0.10 32.541.79 30 5.19 1.24 −0.47 0.10 39.20 11.28 100 11.60 1.79 −0.46 0.08 18.655.90 300 27.98 7.59 −0.34 0.20 14.10 10.79 1000 48.47 8.31 −0.51 0.27−37.01 7.09 Note: Bolded values are significantly different from therespective control means For activation: 3 × SD of vehicle control mean(HBPS) = 2.65; values > 2.65 are significant For positive allostericmodulation: 3 × SD of agonist mean (30 μM Ach) = 19.00; values > 19.00are significant For inhibition: 3 × SD of agonist with the positiveallosteric modulation mean (300 μM Ach + 10 μM PNU) = 28.86; values >28.86 are significant

TABLE 59 Positive Controls Normalized % Channel Test Article ID signalsSD Nicotinic α7 30 μM Ach + 10 μM 100 1.10 (activation) PNU-120596 HBPS0 0.88 Z Prime = 0.50 Nicotinic α7 30 μM Ach + 10 μM 100 6.33(potentiation) PNU-120596 30 μM Ach 0 0.21 Z Prime = 0.80 Nicotinic α7300 μM Ach + 10 μM 0 9.62 (inhibition) PNU-120596 300 μM Ach + 10 μM 1007.46 PNU-120596 + 10 μM MLA Z Prime = 0.49

Discussion and Conclusions

In this study, the ability of nicotine (−) isomer and anatabine racemateto act as agonists, positive allosteric modulators or antagonists ofthree nAChR receptor channels was evaluated. Both test articles wereevaluated for responses on the α3/β4, α4/β2 and α7 nAChR channels ateight (8) concentrations with four (4) replicates for eachconcentration.

In the agonist assay, both test articles increased all three nAChRchannel signals in a concentration-dependent manner indicating that thetest articles were agonists. The nicotine (−) isomer showed the highestactivity towards the nAChR α4/β2 channel (EC₅₀=1.302 μM), followed bythe nAChR α3/β4 channel (EC₅₀=27.78 μM). The EC₅₀ of nicotine for thenAChR 7 channel could not be determined as maximal stimulation was notachieved within the range of concentrations tested.

The EC₅₀ for the anatabine racemate could only be determined for thenAChR (EC₅₀=282 μM) as the maximum level of stimulation was not achievedor could not be determined for the nAChR α3/β4 and nAChR α7 receptor.From these results it can be concluded that the nicotine (−) isomer is amore potent agonist than the anatabine racemate of both the α4/β2 andα3/β4 nAChR channels. The relative agonist potency of the two testarticles towards the α7 receptor could not be established. Nevertheless,it is possible to conclude that anatabine is an agonist of all threechannels, and in particular of the α4/β2 subtype. It is not possible todetermine if anatabine has partial agonist activity towards the α3/β4and α7 channels as a higher concentration range would need to beevaluated so that the level of maximal stimulation can be clearlyidentified.

In the potentiation assay, the test articles did not increase thesignals with a low dose of Ach stimulation indicating that the testarticles were not potentiators or allosteric modulators of the channels.

In the antagonist assay, after stimulation with high dose of Ach, thetest articles decreased the Ach-induced signals. However, since the testarticles acted as agonists, the reduction of Ach-induced signals wascaused by the desensitization of the channels themselves, rather thanthe channel blockage. Nicotine and anatabine are not considered to beantagonists of these receptors.

EXAMPLE 9 Anatabine Reduces BACE-1 mRNA Levels In Vitro

The effect of anatabine (“RCP006”) on BACE-1 mRNA levels in SHSY cellswas measured by RTPCR quantification using standard methodologies.

The effect of anatabine (30 minutes) on BACE-1 mRNA expression in humanneuronal SHSY cells is shown in FIG. 33. TNF-α was used to increase BACEexpression. Anatabine reduced this signal in a concentration-dependentmanner.

FIG. 34 shows the effect of anatabine (24 hours) on BACE-1 proteinexpression in human neuronal SHSY cells, corrected for actin expression.Increasing concentrations of anatabine reduced BACE expression.

These results demonstrate that anatabine can reduce BACE expressionlevels and suggest a mechanism by which anatabine could lower Aβproduction.

EXAMPLE 10 Anatabine Reduces Aβ Production In Vitro

The effect of anatabine (“RCP006”) on Aβ production in vitro in 7W CHOcells was measured. The results are shown in FIG. 35A and FIG. 35B. Bothgraphs show a concentration-dependent reduction of Aβ production byanatabine.

EXAMPLE 11 Anatabine Reduces β-Cleavage of APP In Vitro

The effect of anatabine (“RCP006”) on sAPPβ/sAPPα production in vitrowas measured in 7W CHO cells. The results are shown in FIG. 36. Theseresults demonstrate that anatabine reduces the sAPPβ/sAPPα ratio, whichsuggests that anatabine can lower the activity of BACE to cleave APP. Notoxicity was observed; see FIG. 37.

EXAMPLE 12 Anatabine Reduces p65 Phosphorylation In Vivo

Wild-type mice (B6/SJL), 75 weeks of age, were injectedintraperitoneally with PBS or with 2 mg/kg of anatabine (“RCP006”).After 5 minutes, mice were intracranially injected with 0.5 mg of TNFα.Mice were euthanized ten minutes after the intracranial injection. Theportion of the brain surrounding the intracranial site of injection wascollected, and proteins were extracted. Phosphorylation of p65 wasmeasured with an antibody towards phosphorylated p65.

The results are shown in FIG. 38, normalized to an actin signal. Theseresults demonstrate that anatabine treatment results in reduced p65phosphorylation in mouse brain.

EXAMPLE 13 Anatabine Inhibits LPS-Induced IL-1β Release in Whole HumanBlood

Whole human blood was treated with LPS to stimulate inflammatoryresponses. LPS treatment was also accompanied by treatment with LIPITOR®or with anatabine (“RCP006”). The inflammatory molecule IL-1β wasmeasured after 16 hours.

The results are shown in FIG. 39. A reduced accumulation of IL-1β wasobserved in anatabine-treated blood compared to untreated blood, whereasLIPITOR® had no effect at the dose shown.

EXAMPLE 14 Anatabine Reduces LPS-Induced IL-1β Release in Whole HumanBlood

Whole human blood was treated with LPS to stimulate inflammatoryresponses. LPS treatment was also accompanied by treatment with knownanti-inflammatory compounds or with anatabine (“RCP006”). Theinflammatory molecule IL-1β was measured after 16 hours.

The results are shown in FIG. 40. The data shown were generated bysumming the area under the curve for the dose response (measured inIL-1β levels) from zero to the treatment where full inhibition wasachieved for each compound.

A reduced accumulation of IL-1β in anatabine-treated blood was observed,whereas the commonly used anti-inflammatory agents all triggered anincrease in IL-1β production at lower doses prior to declines at higherdoses. These data are consistent with anatabine having anti-inflammatoryeffects in human blood.

EXAMPLE 15 Anatabine Rapidly and Continuously Suppresses IL-1βProduction in Human Blood

Accumulation of IL-1β was measured repeatedly over time with and withoutanatabine (“RCP006”) treatment, using methods of Examples 13 and 14. Theresults are shown in FIG. 41.

These results demonstrate that anatabine has a rapid and continuouseffect on the suppression if IL-1β production after LPS stimulation ofhuman blood.

EXAMPLE 16A Effects of Anatabine in a Mouse Model of AutoimmuneThyroiditis

Effects of anatabine were studied in a mouse model of autoimmunethyroiditis (Experimental Autoimmune Thyroiditis; EAT). Thyroiditis wasinduced by injection of thyroglobulin emulsified in complete Freund'sadjuvant (CFA). On days 0 and 7, female mice received subcutaneousinjection of 100 μg thyroglobulin (2 injections of 50 μg each). Controlmice drank water. Anatabine-treated mice were provided with watercontaining anatabine (0.05 mg/ml; approximately 12.5 mg/kg bodyweight/day). Mice were sacrificed on day 21.

Thyroid histopathology. Thyroid glands were removed. One lobe was fixedin formalin for histopathology. One lobe was frozen forimmunohistochemistry. The extent of lymphocytic infiltration anddestruction of the thyroid gland was assessed digitally. Initially, theentire thyroid lobe was examined. Then, all regions that showedpathological damage were selected. The final score was expressed as thepercent of the thyroid area infiltrated by lymphocytes and damaged. Theresults are shown graphically in FIG. 42. Anatabine-treated micedeveloped less severe thyroiditis than control mice (p=0.05).Photomicrographs of hematoxylin- and eosin-stained thyroids from controland anatabine-treated mice are shown in FIG. 43A (control) and FIG. 43B(anatabine-treated).

Immunochemistry. Serum from control and anatabine-treated mice wasexamined to determine levels of antibodies to a foreign antigen (PPD).The results are shown in FIG. 44. There was no significant differencebetween the control and anatabine-treated mice.

Levels of antibodies to thyroglobulin were examined on days 7, 14, and21 after immunization. There was no significant difference between thecontrol and anatabine-treated mice at day 7 (FIG. 45). Anatabine-treatedmice tended to have lower thyroglobulin antibodies by day 14 (FIG. 46;p=0.086); by day 21, there was no significant difference between thecontrol and the anatabine-treated mice (FIG. 47).

Lymphoid typing. Cervical lymph nodes were removed for lymphoid typingby flow cytometry. Spleen and peritoneal macrophages were removed for exvivo stimulation. Anatabine-treated mice seemed to have fewer activatedT cells (FIG. 48; p=0.0143), more regulatory T cells (FIG. 49;p=0.0143), and a lower ability to present antigens (FIG. 50; p=0.0143).

EXAMPLE 16B Effects of Anatabine in a Mouse Model of AutoimmuneThyroiditis

In another experiment, eighteen CBA/J female mice were immunized withmouse thyroglobulin, emulsified in complete Freund's adjuvant, on day 0and day 7. One group of mice (n=10) drank regular water. The other groupdrank water supplemented with anatabine (0.05 mg/ml; approximately 12.5mg/kg body weight/day). Mice were sacrificed 21 days after the firstimmunization to collect the thyroid gland and the blood. The thyroid wasanalyzed for the presence of infiltrating mononuclear cells. The bloodwas analyzed for the levels of antibodies against thyroglobulin.

The results are shown in FIG. 51. Mice that drank anatabine developedthyroiditis less frequently and of lower severity (p=0.023 by Wilcoxonrank sum test). Anatabine had no effect on the levels of thyroglobulinantibodies, which increased in both groups after immunization.

EXAMPLE 17 Effect of S-(−)-anatabine on TNFα-Induced NFκB Activity InVitro

The effect of S-(−)-anatabine on TNFα-induced NFκB activity in vitro wasdetermined as described in Example 1. NFκB activity was stimulated with20 ng/ml of TNFα, then varying doses of a racemic mixture of anatabineor S(−)-anatabine were applied to the challenged cells. The data wereplotted as a percentage of the TNFα-induced NFκB activity and are shownin FIG. 52. In this assay the IC₅₀ for the racemic mixture of anatabineis approximately 600 μg/ml, whereas the IC₅₀ for the (S)-enantiomer isapproximately 330 μg/ml.

1. A method of reducing a symptom in an individual of a disordercomprising an NFκB-mediated inflammatory component, comprisingadministering to the individual a composition comprising atherapeutically effective dose of an isolated form of a compound ofFormula I

wherein: R represents hydrogen or C₁-C₅ alkyl; R′ represents hydrogen orC₁-C₇ alkyl; and X represents halogen or C₁-C₇ alkyl, or a salt thereof.2. The method of claim 1 wherein the compound is anatabine orS-(−)-anatabine.
 3. The method of claim 1 wherein the compositioncomprises a salt of anatabine or S-(−)-anatabine.
 4. The method of claim1 wherein the NFκB-mediated inflammatory component is chronicinflammation.
 5. The method of claim 1 wherein the disorder is selectedfrom the group consisting of an autoimmune disorder, a vascularinflammatory disorder, a gastrointestinal inflammatory disorder, aneurodegenerative disorder, cancer, an upper respiratory tractinfection, a joint disorder, seizure disorder, and an autism spectrumdisorder.
 6. The method of claim 5 wherein the disorder is an autoimmunedisorder and the autoimmune disorder is selected from the groupconsisting of thyroiditis, rheumatoid arthritis, and diabetes.
 7. Themethod of claim 5 wherein the disorder is a vascular inflammatorydisorder and the vascular inflammatory disorder is selected from thegroup consisting of atherosclerosis, coronary artery disease,cerebrovascular disease, peripheral vascular disease, andinflammation-induced myocarditis.
 8. The method of claim 5 wherein thedisorder is a neurodegenerative disorder and the neurodegenerativedisorder is selected from the group consisting of Alzheimer's diseaseand Parkinson's disease, and wherein the compound of Formula I isS-(−)-anatabine.
 9. The method of claim 5 wherein the disorder is acancer.
 10. The method of claim 5 wherein the disorder is an upperrespiratory tract infection and the upper respiratory tract infection isa cold.
 11. The method of claim 5 wherein the disorder is a jointdisorder and the joint disorder is selected from the group consisting ofosteoarthritis and degenerative joint disease.
 12. The method of claim 5wherein the disorder is a seizure disorder or an autism spectrumdisorder.
 13. The method of claim 1 wherein the dose is in an extendedrelease formulation.
 14. The method of claim 1 wherein the dose is fromabout 0.1 to about 1.5 mg/kg body weight.
 15. The method of claim 1further comprising administration of a second therapeutic agent.
 16. Amethod of reducing a risk in an individual of developing a disordercomprising an NFκB-mediated inflammatory component, comprisingadministering to the individual a composition comprising atherapeutically effective dose of an isolated form of a compound ofFormula I or a salt thereof.
 17. A beverage product suitable for humanconsumption comprising a beverage container containing a liquid mediumand an isolated form of a compound of Formula I

wherein: R represents hydrogen or C₁-C₅ alkyl; R′ represents hydrogen orC₁-C₇ alkyl; and X represents halogen or C₁-C₇ alkyl, or a salt thereof.18. The beverage product of claim 17 wherein the compound is anatabineor S-(−)-anatabine.
 19. A consumer product selected from the groupconsisting of paste, cream, lotion, moisturizer, sunscreen, toothpaste,mouthwash, and an inhaler, wherein the product contains an isolated formof a compound of Formula I:

wherein: R represents hydrogen or C₁-C₅ alkyl; R′ represents hydrogen orC₁-C₇ alkyl; and X represents halogen or C₁-C₇ alkyl, or a salt thereof.20. The consumer product of claim 19 wherein the compound is anatabineor S-(−)-anatabine.